Variant report

Variant	nsv538318
Chromosome Location	chr6:76306100-76759397
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3569)
CpG islands
(count:2079)
Chromatin interactive
region (count:269)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:3569 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:76339500-76339892	K562	blood:	n/a	n/a
2	ARID3A	chr6:76601370-76601603	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:76458622-76458651	K562	blood:	n/a	n/a
4	ARID3A	chr6:76457201-76457496	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:76484978-76485281	K562	blood:	n/a	n/a
6	ARID3A	chr6:76562512-76562787	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:76337921-76337975	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:76445315-76446019	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:76458528-76458682	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:76331504-76331869	K562	blood:	n/a	n/a
11	ARID3A	chr6:76532773-76532821	HepG2	liver:	n/a	n/a
12	ARID3A	chr6:76342477-76343204	K562	blood:	n/a	chr6:76342662-76342678
13	ARID3A	chr6:76383585-76383961	HepG2	liver:	n/a	n/a
14	ARID3A	chr6:76312666-76313021	K562	blood:	n/a	n/a
15	ARID3A	chr6:76315396-76315502	K562	blood:	n/a	n/a
16	ARID3A	chr6:76333004-76333194	K562	blood:	n/a	n/a
17	ARID3A	chr6:76311201-76311902	HepG2	liver:	n/a	n/a
18	ARID3A	chr6:76313655-76313921	K562	blood:	n/a	n/a
19	ARID3A	chr6:76322881-76323353	HepG2	liver:	n/a	n/a
20	ARID3A	chr6:76320480-76320552	K562	blood:	n/a	n/a
21	ARID3A	chr6:76643375-76643655	HepG2	liver:	n/a	n/a
22	ATF1	chr6:76757267-76757352	K562	blood:	n/a	n/a
23	ATF1	chr6:76562615-76562871	K562	blood:	n/a	n/a
24	ATF1	chr6:76517943-76518107	K562	blood:	n/a	n/a
25	ATF1	chr6:76342790-76343022	K562	blood:	n/a	n/a
26	ATF2	chr6:76540581-76541147	GM12878	blood:	n/a	n/a
27	ATF2	chr6:76703028-76703778	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr6:76636098-76636563	GM12878	blood:	n/a	n/a
29	ATF2	chr6:76311636-76312501	GM12878	blood:	n/a	n/a
30	ATF2	chr6:76540625-76541135	GM12878	blood:	n/a	n/a
31	ATF3	chr6:76400719-76401129	HCT-116	colon:	n/a	n/a
32	BACH1	chr6:76311710-76311864	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr6:76318040-76318256	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr6:76603125-76603698	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr6:76459213-76459671	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr6:76458435-76458631	K562	blood:	n/a	n/a
37	BACH1	chr6:76312675-76312783	K562	blood:	n/a	n/a
38	BACH1	chr6:76644723-76645282	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr6:76523240-76523470	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr6:76407134-76407232	K562	blood:	n/a	n/a
41	BACH1	chr6:76458387-76458719	H1-hESC	embryonic stem cell:	n/a	n/a
42	BATF	chr6:76468871-76469148	GM12878	blood:	n/a	chr6:76468983-76468994
43	BATF	chr6:76540656-76541080	GM12878	blood:	n/a	chr6:76540850-76540861 chr6:76540956-76540965 chr6:76540847-76540857
44	BATF	chr6:76491591-76491869	GM12878	blood:	n/a	chr6:76491779-76491789
45	BATF	chr6:76540606-76541165	GM12878	blood:	n/a	chr6:76540850-76540861 chr6:76540956-76540965 chr6:76540847-76540857
46	BATF	chr6:76641889-76642089	GM12878	blood:	n/a	n/a
47	BATF	chr6:76713845-76714245	GM12878	blood:	n/a	chr6:76714006-76714015
48	BATF	chr6:76636006-76636350	GM12878	blood:	n/a	n/a
49	BATF	chr6:76713883-76714156	GM12878	blood:	n/a	chr6:76714006-76714015
50	BATF	chr6:76453741-76453966	GM12878	blood:	n/a	n/a

(count:2079 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:76655983-76656033	NB4	blood:	n/a
2	chr6:76425457-76425507	BJ	skin:	n/a
3	chr6:76315197-76315247	Hepatocyte	liver:	n/a
4	chr6:76310551-76310601	NT2-D1	testis:	n/a
5	chr6:76459077-76459127	SKMC	muscle:	n/a
6	chr6:76655983-76656033	NB4	blood:	n/a
7	chr6:76425457-76425507	BJ	skin:	n/a
8	chr6:76315197-76315247	Hepatocyte	liver:	n/a
9	chr6:76310551-76310601	NT2-D1	testis:	n/a
10	chr6:76459077-76459127	SKMC	muscle:	n/a
11	chr6:76702942-76702992	IMR90	lung:	fetal
12	chr6:76425457-76425507	HEEpiC	esophagus:	n/a
13	chr6:76603364-76603414	HMEC	breast:	n/a
14	chr6:76311636-76311686	NHBE	bronchial:	n/a
15	chr6:76644222-76644272	NHBE	bronchial:	n/a
16	chr6:76636725-76636775	AoSMC	blood vessel:	n/a
17	chr6:76655983-76656033	GM12892	blood:	n/a
18	chr6:76312378-76312428	HAEpiC	amniotic membrane:	n/a
19	chr6:76631383-76631433	NHBE	bronchial:	n/a
20	chr6:76311636-76311686	ovcar-3	ovarian:	n/a
21	chr6:76645016-76645066	ovcar-3	ovarian:	n/a
22	chr6:76724431-76724481	NH-A	brain:	n/a
23	chr6:76459511-76459561	HCF	heart:	n/a
24	chr6:76309300-76309350	MCF10A-Er-Src	breast:	n/a
25	chr6:76644222-76644272	SKMC	muscle:	n/a
26	chr6:76724431-76724481	GM19239	blood:	n/a
27	chr6:76696290-76696340	Hela-S3	cervix:	n/a
28	chr6:76311636-76311686	HPAEpiC	pulmonary alveolar:	n/a
29	chr6:76631383-76631433	AG10803	skin:	n/a
30	chr6:76645016-76645066	HRCEpiC	kidney:	n/a
31	chr6:76644222-76644272	HRCEpiC	kidney:	n/a
32	chr6:76425457-76425507	HAEpiC	amniotic membrane:	n/a
33	chr6:76459511-76459561	GM12878	blood:	n/a
34	chr6:76644222-76644272	AoSMC	blood vessel:	n/a
35	chr6:76631383-76631433	HRCEpiC	kidney:	n/a
36	chr6:76645008-76645058	GM06990	blood:	n/a
37	chr6:76724431-76724481	AoSMC	blood vessel:	n/a
38	chr6:76311363-76311413	SKMC	muscle:	n/a
39	chr6:76425457-76425507	ECC-1	luminal epithelium:	n/a
40	chr6:76311920-76311970	HCT-116	colon:	n/a
41	chr6:76645123-76645173	HIPEpiC	eye:	n/a
42	chr6:76311920-76311970	GM06990	blood:	n/a
43	chr6:76341733-76341783	SKMC	muscle:	n/a
44	chr6:76456187-76456237	PrEC	prostate:	n/a
45	chr6:76311363-76311413	NH-A	brain:	n/a
46	chr6:76645016-76645066	MCF-7	breast:	n/a
47	chr6:76309300-76309350	HepG2	liver:	n/a
48	chr6:76644790-76644840	ECC-1	luminal epithelium:	n/a
49	chr6:76655983-76656033	HL-60	blood:	n/a
50	chr6:76312378-76312428	Jurkat	blood:	n/a

(count:269 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr6:76461468..76463754-chr6:76469518..76472253,2	MCF-7	breast:
2	chr6:76404187..76405990-chr6:76505413..76507332,2	MCF-7	breast:
3	chr6:76348163..76350859-chr6:76356641..76358719,2	K562	blood:
4	chr6:76341666..76343684-chr6:76358850..76361030,2	K562	blood:
5	chr6:76310839..76313480-chr6:76354672..76356986,2	MCF-7	breast:
6	chr6:76423467..76426296-chr6:76461021..76463732,3	MCF-7	breast:
7	chr6:76424657..76427289-chr6:76428050..76430901,3	MCF-7	breast:
8	chr6:76457614..76459414-chr6:76469003..76470756,2	K562	blood:
9	chr6:76469142..76471151-chr6:76480358..76482124,2	MCF-7	breast:
10	chr6:76602974..76603706-chr6:76641806..76642424,2	MCF-7	breast:
11	chr6:76311042..76312955-chr6:76326997..76330794,3	MCF-7	breast:
12	chr6:76402073..76403999-chr6:76420565..76422699,2	MCF-7	breast:
13	chr6:76620793..76623567-chr6:76626394..76629286,2	MCF-7	breast:
14	chr6:76369470..76371755-chr6:76372281..76373933,2	K562	blood:
15	chr3:150479690..150481282-chr6:76352345..76354574,2	MCF-7	breast:
16	chr6:76337128..76338933-chr6:76358786..76360573,2	K562	blood:
17	chr6:76423793..76426485-chr6:76434093..76435596,2	K562	blood:
18	chr6:76337128..76338933-chr6:76358786..76360573,2	K562	blood:
19	chr6:76459743..76462264-chr6:76558072..76560658,3	MCF-7	breast:
20	chr6:76467679..76469997-chr6:76472807..76474955,2	K562	blood:
21	chr6:76309895..76312807-chr6:76370964..76372976,2	K562	blood:
22	chr6:74405547..74407236-chr6:76311267..76312799,2	MCF-7	breast:
23	chr17:56735238..56737884-chr6:76312067..76314109,2	MCF-7	breast:
24	chr6:76354799..76357581-chr6:76387845..76390206,2	K562	blood:
25	chr6:75993176..75995308-chr6:76310710..76312367,2	MCF-7	breast:
26	chr6:76325725..76327529-chr6:76327837..76330229,2	K562	blood:
27	chr6:74229402..74231607-chr6:76310929..76313785,2	K562	blood:
28	chr6:76467679..76469997-chr6:76472807..76474955,2	K562	blood:
29	chr6:76310252..76312972-chr6:76331195..76334683,3	MCF-7	breast:
30	chr6:76467657..76469847-chr6:76559756..76561654,2	MCF-7	breast:
31	chr6:76620793..76623567-chr6:76626394..76629286,2	MCF-7	breast:
32	chr6:41039866..41042611-chr6:76456761..76459603,2	MCF-7	breast:
33	chr6:76402029..76404149-chr6:76408590..76410105,2	MCF-7	breast:
34	chr6:76711975..76713621-chr6:76719761..76721754,2	K562	blood:
35	chr6:76465017..76467292-chr6:76472497..76474825,2	K562	blood:
36	chr6:76458866..76461215-chr6:76472496..76475519,3	MCF-7	breast:
37	chr6:76655935..76657484-chr6:76657598..76659631,2	MCF-7	breast:
38	chr6:75992888..75995675-chr6:76335735..76338499,2	K562	blood:
39	chr6:76458766..76460644-chr6:76463670..76465363,2	MCF-7	breast:
40	chr6:76310966..76312781-chr6:76360511..76362036,2	MCF-7	breast:
41	chr6:76424414..76426953-chr6:76430333..76433018,2	MCF-7	breast:
42	chr6:76311833..76313694-chr6:76456932..76459481,3	MCF-7	breast:
43	chr6:76327800..76329805-chr6:76331383..76333611,2	K562	blood:
44	chr6:76446062..76448644-chr6:76456702..76459457,3	MCF-7	breast:
45	chr6:76298381..76301021-chr6:76312234..76315010,2	K562	blood:
46	chr6:76641897..76642417-chr6:77570899..77571594,2	MCF-7	breast:
47	chr11:93474252..93474772-chr6:76458412..76459090,2	Hela-S3	cervix:
48	chr6:76316110..76319023-chr6:76339771..76341687,2	K562	blood:
49	chr6:76467657..76469847-chr6:76559756..76561654,2	MCF-7	breast:
50	chr6:76459743..76462264-chr6:76558072..76560658,3	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYO6-6	chr6:76357008-76357517	NONHSAT113627
2	lnc-MYO6-7	chr6:76343366-76343442	NONHSAT113624
3	lnc-FILIP1-3	chr6:76364686-76365015	NONHSAT113628
4	lnc-FILIP1-2	chr6:76320906-76321661	NONHSAT113623
5	lnc-MYO6-1	chr6:76359931-76362040	ENSG00000249080
6	lnc-MYO6-4	chr6:76673631-76673965	expReg_chr6_7326_+
7	lnc-MYO6-6	chr6:76372937-76373221	NONHSAT113627
8	lnc-SENP6-5	chr6:76434955-76435356	NONHSAT113632
9	lnc-MYO6-6	chr6:76368978-76369123	NONHSAT113627
10	lnc-SENP6-4	chr6:76433669-76434665	NONHSAT113631
11	lnc-MYO6-1	chr6:76362140-76362390	ENSG00000249080
12	lnc-MYO6-7	chr6:76344423-76344772	NONHSAT113624
13	lnc-FILIP1-2	chr6:76320674-76321504	NONHSAT113622

No data

(count:6 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	MYO6	hsa-miR-145-5p	chr6:76625103-76625109
2	MYO6	hsa-miR-143-3p	chr6:76625556-76625576
3	MYO6	hsa-miR-143-3p	chr6:76625569-76625576
4	MYO6	hsa-miR-320a	chr6:76625812-76625831
5	MYO6	hsa-miR-145-5p	chr6:76625088-76625110
6	MYO6	hsa-miR-145-5p	chr6:76625538-76625544

Variant related genes	Relation type
RN7SKP163	TF binding region
SENP6	TF binding region
IMPG1	TF binding region
ENSG00000200040	TF binding region
MYO6	TF binding region
RNU6-1016P	TF binding region
ENSG00000217488	TF binding region
ENSG00000239132	TF binding region
RNU6-155P	TF binding region
RNA5SP209	TF binding region
RN7SKP163	CpG island
SENP6	CpG island
IMPG1	CpG island
ENSG00000200040	CpG island
MYO6	CpG island
RNU6-1016P	CpG island
ENSG00000217488	CpG island
ENSG00000239132	CpG island
RNU6-155P	CpG island
RNA5SP209	CpG island
ENSG00000196586	chromatin interactions
ENSG00000166012	chromatin interactions
ENSG00000112695	chromatin interactions
ENSG00000101447	chromatin interactions
ENSG00000112701	chromatin interactions
ENSG00000204120	chromatin interactions
ENSG00000182919	chromatin interactions
ENSG00000143971	chromatin interactions
ENSG00000267598	chromatin interactions
ENSG00000252498	chromatin interactions
ENSG00000252156	chromatin interactions
ENSG00000164430	chromatin interactions
ENSG00000123505	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000167470	chromatin interactions
ENSG00000112697	chromatin interactions
ENSG00000223169	chromatin interactions
ENSG00000108854	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000181788	chromatin interactions
ENSG00000220730	chromatin interactions
ENSG00000239132	chromatin interactions
ENSG00000244265	chromatin interactions
ENSG00000229862	chromatin interactions
ENSG00000155903	chromatin interactions
ENSG00000100888	chromatin interactions
ENSG00000156535	chromatin interactions
ENSG00000231652	chromatin interactions
ENSG00000001167	chromatin interactions
ENSG00000225793	chromatin interactions
ENSG00000217488	chromatin interactions
ENSG00000252137	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000124596	chromatin interactions
ENSG00000169715	chromatin interactions
KRAS	miRNA target sites
NR4A2	miRNA target sites

Extended variants
information (count: 15221 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:15221 , 50 per page) page: 1 2 3 4 5 6 7 ... 305

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147680051	chr6:76306103-76306104	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs564902675	chr6:76306157-76306158	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs73752614	chr6:76306166-76306167	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs577756673	chr6:76306207-76306208	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs182292277	chr6:76306233-76306234	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs150279803	chr6:76306243-76306244	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs573029391	chr6:76306246-76306247	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs530309053	chr6:76306265-76306266	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs187869489	chr6:76306274-76306275	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs566541734	chr6:76306322-76306323	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs533835718	chr6:76306341-76306342	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs191011397	chr6:76306345-76306346	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs183315475	chr6:76306379-76306380	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs538187106	chr6:76306398-76306399	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs556413194	chr6:76306421-76306422	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs574580047	chr6:76306422-76306423	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs541984617	chr6:76306437-76306438	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs553656649	chr6:76306445-76306446	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs573017606	chr6:76306448-76306449	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs591467	chr6:76306462-76306463	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs564940470	chr6:76306465-76306466	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs532371046	chr6:76306473-76306474	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs544621308	chr6:76306475-76306476	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs375133748	chr6:76306495-76306496	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs529094768	chr6:76306496-76306497	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs188253715	chr6:76306511-76306512	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs375148159	chr6:76306523-76306524	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs191996842	chr6:76306526-76306527	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs184458246	chr6:76306578-76306579	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs149409863	chr6:76306583-76306584	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs187723269	chr6:76306603-76306604	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs552295004	chr6:76306610-76306611	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs192686346	chr6:76306630-76306631	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs184143974	chr6:76306632-76306633	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs537825205	chr6:76306648-76306649	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs189523911	chr6:76306649-76306650	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs577782008	chr6:76306653-76306654	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs77614579	chr6:76306654-76306655	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs75981095	chr6:76306655-76306656	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs531870467	chr6:76306703-76306704	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs550171178	chr6:76306715-76306716	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs535354360	chr6:76306722-76306723	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs6453835	chr6:76306750-76306751	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs192611895	chr6:76306753-76306754	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs540374398	chr6:76306790-76306791	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs558620425	chr6:76306796-76306797	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs547780680	chr6:76306857-76306858	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs184806393	chr6:76306861-76306862	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs566412230	chr6:76306944-76306945	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs143745285	chr6:76306967-76306968	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Salivary gland tumor	18059337	CNVD
Lung cancer	16773561	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial cell carcinoma	18451213	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:7165 , 50 per page) page: 1 2 3 4 5 6 7 ... 144

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:76305600-76306200	Enhancers	Fetal Intestine Small	intestine
2	chr6:76305600-76306800	Enhancers	HepG2	liver
3	chr6:76306000-76310000	Weak transcription	Fetal Intestine Large	intestine
4	chr6:76306200-76309000	Weak transcription	Fetal Intestine Small	intestine
5	chr6:76306600-76306800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
6	chr6:76306600-76307800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr6:76306600-76308200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr6:76306600-76308200	Enhancers	Colon Smooth Muscle	Colon
9	chr6:76306800-76307600	Enhancers	Primary B cells from peripheral blood	blood
10	chr6:76306800-76307600	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr6:76306800-76308000	Enhancers	Duodenum Smooth Muscle	Duodenum
12	chr6:76306800-76308200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
13	chr6:76306800-76308200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr6:76306800-76308400	Enhancers	Rectal Smooth Muscle	rectum
15	chr6:76306800-76310400	Weak transcription	HepG2	liver
16	chr6:76307000-76308200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr6:76307200-76308200	Enhancers	Primary T helper naive cells from peripheral blood	blood
18	chr6:76307200-76308200	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr6:76307200-76308600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr6:76307400-76307600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
21	chr6:76307400-76308400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr6:76307400-76308400	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr6:76307400-76308400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr6:76307600-76308000	Weak transcription	Primary B cells from peripheral blood	blood
25	chr6:76307600-76308600	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr6:76307800-76309000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr6:76307800-76309200	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr6:76308000-76308400	Enhancers	Primary B cells from peripheral blood	blood
29	chr6:76308000-76308600	Enhancers	Duodenum Mucosa	Duodenum
30	chr6:76308000-76308800	Active TSS	Aorta	Aorta
31	chr6:76308000-76308800	Active TSS	Duodenum Smooth Muscle	Duodenum
32	chr6:76308000-76309200	Active TSS	Stomach Smooth Muscle	stomach
33	chr6:76308200-76308400	Enhancers	Primary hematopoietic stem cells	blood
34	chr6:76308200-76308400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
35	chr6:76308200-76308400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr6:76308200-76308400	Flanking Active TSS	Colon Smooth Muscle	Colon
37	chr6:76308200-76308400	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr6:76308200-76308600	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chr6:76308200-76308600	Enhancers	Brain Angular Gyrus	brain
40	chr6:76308200-76308800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
41	chr6:76308200-76308800	Active TSS	Ovary	ovary
42	chr6:76308200-76309000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
43	chr6:76308200-76309000	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
44	chr6:76308200-76309000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
45	chr6:76308200-76309000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
46	chr6:76308200-76309000	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr6:76308400-76308600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr6:76308400-76308800	Flanking Active TSS	Primary B cells from peripheral blood	blood
49	chr6:76308400-76308800	Active TSS	Primary T cells fromperipheralblood	blood
50	chr6:76308400-76308800	Active TSS	Primary T helper cells PMA-I stimulated	--

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