Variant report

Variant	nsv461546
Chromosome Location	chr4:69049643-69223057
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1676)
CpG islands
(count:2076)
Chromatin interactive
region (count:76)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:1676 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69165746-69166230	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69133011-69133899	K562	blood:	n/a	n/a
3	ARID3A	chr4:69215712-69215831	K562	blood:	n/a	chr4:69215782-69215790
4	ARID3A	chr4:69215585-69216036	HepG2	liver:	n/a	chr4:69215782-69215790
5	ARID3A	chr4:69210304-69210353	K562	blood:	n/a	n/a
6	ARID3A	chr4:69130002-69130028	K562	blood:	n/a	n/a
7	ARID3A	chr4:69185567-69186004	K562	blood:	n/a	n/a
8	ARID3A	chr4:69212206-69212462	HepG2	liver:	n/a	n/a
9	ATF1	chr4:69133136-69133799	K562	blood:	n/a	n/a
10	ATF1	chr4:69121959-69122424	K562	blood:	n/a	n/a
11	ATF1	chr4:69131895-69132155	K562	blood:	n/a	n/a
12	ATF1	chr4:69215620-69216158	K562	blood:	n/a	chr4:69215838-69215852
13	ATF1	chr4:69130896-69131204	K562	blood:	n/a	n/a
14	ATF1	chr4:69212269-69212558	K562	blood:	n/a	n/a
15	ATF2	chr4:69215430-69216233	H1-hESC	embryonic stem cell:	n/a	chr4:69215896-69215907 chr4:69215838-69215852
16	ATF2	chr4:69215452-69216129	GM12878	blood:	n/a	chr4:69215896-69215907 chr4:69215838-69215852
17	ATF2	chr4:69215463-69216132	H1-hESC	embryonic stem cell:	n/a	chr4:69215896-69215907 chr4:69215838-69215852
18	ATF2	chr4:69215580-69216036	GM12878	blood:	n/a	chr4:69215896-69215907 chr4:69215838-69215852
19	ATF2	chr4:69214914-69215381	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr4:69165597-69165751	K562	blood:	n/a	n/a
21	BACH1	chr4:69215560-69216041	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr4:69106381-69106661	K562	blood:	n/a	n/a
23	BACH1	chr4:69166084-69166208	K562	blood:	n/a	n/a
24	BACH1	chr4:69215649-69216046	K562	blood:	n/a	n/a
25	BACH1	chr4:69100294-69100367	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr4:69165562-69165682	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr4:69207891-69208159	K562	blood:	n/a	n/a
28	BACH1	chr4:69137557-69138352	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr4:69216585-69216762	K562	blood:	n/a	n/a
30	BATF	chr4:69115111-69115437	GM12878	blood:	n/a	chr4:69115296-69115307 chr4:69115376-69115384
31	BATF	chr4:69212238-69212535	GM12878	blood:	n/a	chr4:69212303-69212314 chr4:69212358-69212369
32	BATF	chr4:69212136-69212549	GM12878	blood:	n/a	chr4:69212303-69212314 chr4:69212358-69212369
33	BCL11A	chr4:69115147-69115501	GM12878	blood:	n/a	n/a
34	BCL3	chr4:69215396-69216133	A549	lung:	n/a	n/a
35	BCL3	chr4:69215550-69215963	A549	lung:	n/a	n/a
36	BCLAF1	chr4:69215363-69216070	GM12878	blood:	n/a	n/a
37	BCLAF1	chr4:69215374-69216170	GM12878	blood:	n/a	n/a
38	BHLHE40	chr4:69215129-69216171	HepG2	liver:	n/a	n/a
39	BHLHE40	chr4:69214925-69215208	GM12878	blood:	n/a	n/a
40	BHLHE40	chr4:69215541-69216054	A549	lung:	n/a	n/a
41	BHLHE40	chr4:69121233-69121402	K562	blood:	n/a	n/a
42	BHLHE40	chr4:69205892-69205953	GM12878	blood:	n/a	n/a
43	BHLHE40	chr4:69215413-69216189	GM12878	blood:	n/a	n/a
44	BHLHE40	chr4:69138568-69138734	GM12878	blood:	n/a	n/a
45	BHLHE40	chr4:69212159-69212359	GM12878	blood:	n/a	n/a
46	BHLHE40	chr4:69109982-69110192	GM12878	blood:	n/a	n/a
47	BHLHE40	chr4:69115198-69115451	GM12878	blood:	n/a	n/a
48	BHLHE40	chr4:69151973-69151987	GM12878	blood:	n/a	n/a
49	BHLHE40	chr4:69215383-69216210	K562	blood:	n/a	n/a
50	BRCA1	chr4:69215639-69216176	Hela-S3	cervix:	n/a	n/a

(count:2076 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69179965-69180015	NB4	blood:	n/a
2	chr4:69179965-69180015	CMK	blood:	n/a
3	chr4:69179965-69180015	NB4	blood:	n/a
4	chr4:69179965-69180015	CMK	blood:	n/a
5	chr4:69179935-69179985	HCF	heart:	n/a
6	chr4:69215675-69215725	HL-60	blood:	n/a
7	chr4:69179965-69180015	BE2_C	brain:	n/a
8	chr4:69102304-69102354	NH-A	brain:	n/a
9	chr4:69216103-69216153	A549	lung:	n/a
10	chr4:69216018-69216068	LNCaP	prostate:	n/a
11	chr4:69215896-69215946	HepG2	liver:	n/a
12	chr4:69179965-69180015	Hela-S3	cervix:	n/a
13	chr4:69187090-69187140	SAEC	small airway:	n/a
14	chr4:69111580-69111630	HPAEpiC	pulmonary alveolar:	n/a
15	chr4:69216018-69216068	HEEpiC	esophagus:	n/a
16	chr4:69084723-69084773	T-47D	breast:	n/a
17	chr4:69215993-69216043	Jurkat	blood:	n/a
18	chr4:69218719-69218769	LNCaP	prostate:	n/a
19	chr4:69215920-69215970	CMK	blood:	n/a
20	chr4:69215865-69215915	ProgFib	skin:	n/a
21	chr4:69216018-69216068	CMK	blood:	n/a
22	chr4:69179905-69179955	Hepatocyte	liver:	n/a
23	chr4:69138730-69138780	ovcar-3	ovarian:	n/a
24	chr4:69207281-69207331	SK-N-SH	brain:	n/a
25	chr4:69093675-69093725	CMK	blood:	n/a
26	chr4:69216018-69216068	HCM	heart:	n/a
27	chr4:69216077-69216127	PANC-1	pancreas:	n/a
28	chr4:69187090-69187140	K562	blood:	n/a
29	chr4:69111580-69111630	BE2_C	brain:	n/a
30	chr4:69215265-69215315	GM06990	blood:	n/a
31	chr4:69179935-69179985	ProgFib	skin:	n/a
32	chr4:69176865-69176915	Caco-2	colon:	n/a
33	chr4:69179935-69179985	HMEC	breast:	n/a
34	chr4:69215675-69215725	HRPEpiC	eye:	n/a
35	chr4:69215909-69215959	AG10803	skin:	n/a
36	chr4:69215318-69215368	Hepatocyte	liver:	n/a
37	chr4:69215865-69215915	GM06990	blood:	n/a
38	chr4:69054755-69054805	MCF-7	breast:	n/a
39	chr4:69179935-69179985	MCF10A-Er-Src	breast:	n/a
40	chr4:69215993-69216043	AG10803	skin:	n/a
41	chr4:69083729-69083779	K562	blood:	n/a
42	chr4:69102304-69102354	A549	lung:	n/a
43	chr4:69215920-69215970	MCF10A-Er-Src	breast:	n/a
44	chr4:69215786-69215836	SK-N-MC	brain:	n/a
45	chr4:69215909-69215959	A549	lung:	n/a
46	chr4:69215909-69215959	AG04450	lung:	fetal
47	chr4:69216103-69216153	NHBE	bronchial:	n/a
48	chr4:69216111-69216161	Jurkat	blood:	n/a
49	chr4:69207281-69207331	NB4	blood:	n/a
50	chr4:69187090-69187140	SKMC	muscle:	n/a

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:69211727..69213859-chr4:69233011..69234860,2	MCF-7	breast:
2	chr4:69201801..69210708-chr4:69210917..69216982,18	MCF-7	breast:
3	chr4:69193856..69197351-chr4:69199834..69202897,3	K562	blood:
4	chr4:69104849..69107521-chr4:69108866..69110814,2	K562	blood:
5	chr4:69201801..69210708-chr4:69210917..69216982,18	MCF-7	breast:
6	chr4:69197134..69202591-chr4:69207411..69211710,5	K562	blood:
7	chr4:69211043..69213753-chr4:69341284..69343236,2	K562	blood:
8	chr4:69104849..69107521-chr4:69108866..69110814,2	K562	blood:
9	chr4:69193259..69194902-chr4:69207176..69209237,2	K562	blood:
10	chr4:69184387..69189149-chr4:69189998..69193594,6	K562	blood:
11	chr4:69214165..69216661-chr4:69217166..69218936,2	MCF-7	breast:
12	chr4:68794157..68794866-chr4:69050816..69051359,2	MCF-7	breast:
13	chr4:69148927..69150978-chr4:69199918..69202560,2	K562	blood:
14	chr4:69215315..69216150-chr4:69241399..69242116,2	MCF-7	breast:
15	chr1:40042036..40042680-chr4:69215224..69215736,2	Hela-S3	cervix:
16	chr4:69218178..69222853-chr4:69225128..69229971,4	MCF-7	breast:
17	chr4:69152138..69154955-chr4:69200554..69203200,2	K562	blood:
18	chr4:69178701..69181215-chr4:69184356..69187272,2	K562	blood:
19	chr4:69190188..69191856-chr4:69197482..69199638,2	MCF-7	breast:
20	chr4:69188491..69190589-chr4:69207832..69210150,2	K562	blood:
21	chr4:69213512..69216500-chr4:69770884..69773457,2	MCF-7	breast:
22	chr4:69084812..69087062-chr4:69097475..69100132,2	K562	blood:
23	chr4:69052749..69055570-chr4:69072267..69074922,2	MCF-7	breast:
24	chr1:173836748..173837377-chr4:69215292..69215827,2	Hela-S3	cervix:
25	chr4:69166036..69168976-chr4:69169568..69172495,3	K562	blood:
26	chr4:69188337..69192029-chr4:69196790..69201126,5	K562	blood:
27	chr4:69188150..69190673-chr4:69212848..69214663,2	K562	blood:
28	chr11:62609142..62609643-chr4:69215081..69215921,2	Hela-S3	cervix:
29	chr21:45195495..45196196-chr4:69215418..69216293,2	Hela-S3	cervix:
30	chr4:69152138..69154955-chr4:69200554..69203200,2	K562	blood:
31	chr4:69212970..69215845-chr4:69239349..69242311,2	MCF-7	breast:
32	chr4:69218952..69221343-chr4:69221565..69223660,2	K562	blood:
33	chr4:69218952..69221343-chr4:69221565..69223660,2	K562	blood:
34	chr4:69148927..69150978-chr4:69199918..69202560,2	K562	blood:
35	chr4:69215347..69216165-chr5:72143739..72144575,2	Hela-S3	cervix:
36	chr4:69052749..69055570-chr4:69072267..69074922,2	MCF-7	breast:
37	chr1:180884197..180885718-chr4:69153705..69156603,2	MCF-7	breast:
38	chr4:68794052..68794960-chr4:69050850..69051709,2	MCF-7	breast:
39	chr4:69193259..69194902-chr4:69207176..69209237,2	K562	blood:
40	chr4:69078600..69080157-chr4:69085569..69088456,2	MCF-7	breast:
41	chr4:69188491..69190589-chr4:69207832..69210150,2	K562	blood:
42	chr4:69193689..69197466-chr4:69197800..69202580,8	K562	blood:
43	chr4:69167518..69169573-chr4:69172863..69174669,2	K562	blood:
44	chr4:69143211..69145096-chr4:69239415..69241951,2	K562	blood:
45	chr4:69193668..69196027-chr4:69216381..69218945,2	K562	blood:
46	chr4:69194830..69197133-chr4:69209748..69212433,2	K562	blood:
47	chr4:69210254..69212514-chr4:69233666..69236534,2	MCF-7	breast:
48	chr4:69191125..69192742-chr4:69213707..69216637,2	K562	blood:
49	chr4:69084812..69087062-chr4:69097475..69100132,2	K562	blood:
50	chr4:69190188..69191856-chr4:69197482..69199638,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMPRSS11BNL-1	chr4:69056739-69057034	NONHSAT096727
2	lnc-TMPRSS11BNL-1	chr4:69071594-69071815	NONHSAT096726
3	lnc-YTHDC1-2	chr4:69149523-69149595	NONHSAT096728
4	lnc-TMPRSS11BNL-1	chr4:69071753-69071815	NONHSAT096727
5	lnc-TMPRSS11BNL-1	chr4:69054121-69054474	NONHSAT096726
6	lnc-TMPRSS11BNL-1	chr4:69083624-69083721	NONHSAT096727
7	lnc-TMPRSS11BNL-1	chr4:69078080-69078195	NONHSAT096727
8	lnc-YTHDC1-2	chr4:69151533-69151677	NONHSAT096728
9	lnc-TMPRSS11E-5	chr4:69078024-69078188	NR_015446
10	lnc-TMPRSS11E-5	chr4:69051478-69051601	NR_015446
11	lnc-YTHDC1-1	chr4:69170061-69170657	NONHSAT096730
12	lnc-YTHDC1-2	chr4:69148179-69148398	NONHSAT096728
13	lnc-TMPRSS11BNL-1	chr4:69083624-69083722	NONHSAT096726

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	YTHDC1	hsa-miR-1	chr4:69176388-69176409
2	YTHDC1	hsa-miR-93-5p	chr4:69178020-69178042
3	YTHDC1	hsa-miR-93-5p	chr4:69179594-69179620
4	YTHDC1	hsa-miR-103a-3p	chr4:69179397-69179423
5	YTHDC1	hsa-miR-93-5p	chr4:69178392-69178416
6	YTHDC1	hsa-miR-16-5p	chr4:69179396-69179418

Variant related genes	Relation type
ENSG00000249531	TF binding region
TMPRSS11B	TF binding region
TMPRSS11BNL	TF binding region
ENSG00000248639	TF binding region
YTHDC1	TF binding region
APOOP4	TF binding region
ENSG00000250642	TF binding region
ENSG00000250026	TF binding region
ENSG00000249531	CpG island
TMPRSS11B	CpG island
TMPRSS11BNL	CpG island
ENSG00000248639	CpG island
YTHDC1	CpG island
APOOP4	CpG island
ENSG00000250642	CpG island
ENSG00000250026	CpG island
ENSG00000185278	chromatin interactions
ENSG00000083896	chromatin interactions
ENSG00000248122	chromatin interactions
ENSG00000160213	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000272626	chromatin interactions
ENSG00000250026	chromatin interactions
ENSG00000117450	chromatin interactions
ENSG00000162840	chromatin interactions
ENSG00000083312	chromatin interactions
ENSG00000234741	chromatin interactions
ENSG00000188177	chromatin interactions
ENSG00000090621	chromatin interactions
ENSG00000249531	chromatin interactions

Extended variants
information (count: 5290 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:5290 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11940802	chr4:69049643-69049644	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs4577653	chr4:69049674-69049675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551945393	chr4:69049693-69049694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs571454947	chr4:69049700-69049701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs186092917	chr4:69049718-69049719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs11931973	chr4:69049719-69049720	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs567669480	chr4:69049725-69049726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs536227340	chr4:69049771-69049772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs116153384	chr4:69049798-69049799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577038970	chr4:69049802-69049803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs149585793	chr4:69049808-69049809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs146106237	chr4:69049830-69049831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545794624	chr4:69049831-69049832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs140077661	chr4:69049859-69049860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs572196423	chr4:69049902-69049903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs541108653	chr4:69049924-69049925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs560786405	chr4:69049962-69049963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs191934982	chr4:69049967-69049968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553569471	chr4:69049978-69049979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs199596576	chr4:69049979-69049980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs367780366	chr4:69050012-69050013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184236238	chr4:69050040-69050041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185892743	chr4:69050085-69050086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563608180	chr4:69050098-69050099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532271923	chr4:69050121-69050122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551982203	chr4:69050182-69050183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559729957	chr4:69050195-69050196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540721252	chr4:69050201-69050202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs118067498	chr4:69050208-69050209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs2319879	chr4:69050262-69050263	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs567608599	chr4:69050291-69050292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7669495	chr4:69050299-69050300	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs376146319	chr4:69050322-69050323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200427509	chr4:69050349-69050350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191093398	chr4:69050350-69050351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs57112736	chr4:69050358-69050359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs58039447	chr4:69050359-69050360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570408124	chr4:69050466-69050467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143542426	chr4:69050493-69050494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559226900	chr4:69050497-69050498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2319880	chr4:69050500-69050501	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs373291777	chr4:69050505-69050506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375827253	chr4:69050514-69050515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2319881	chr4:69050515-69050516	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs554650771	chr4:69050543-69050544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574407090	chr4:69050549-69050550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570782124	chr4:69050594-69050595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372393489	chr4:69050630-69050631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556663250	chr4:69050638-69050639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs17590869	chr4:69050703-69050704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	20369283	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Oral cancer	21386901	CNVD
Alcoholism	21790672	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD
small cell lung cancer	20016488	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
Autism	19287141	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Ollier disease	21235737	CNVD
Autism	21865298	CNVD
Rett syndrome	21593744	CNVD
Urothelial carcinoma	21177765	CNVD
Incontinentia Pigmenti	22033527	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Thoracic aortic aneurysm	21698135	CNVD
Breast cancer	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Breast cancer	22522925	CNVD
Medulloblastoma	21163964	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2322 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69048600-69054400	Weak transcription	Esophagus	oesophagus
2	chr4:69048800-69050000	Enhancers	Hela-S3	cervix
3	chr4:69080200-69081000	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr4:69080400-69084200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr4:69080800-69081000	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr4:69080800-69081000	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr4:69081000-69082000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr4:69081000-69082000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr4:69081000-69082200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr4:69081200-69081400	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr4:69082000-69082600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr4:69082000-69083800	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr4:69082000-69084200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr4:69082200-69082400	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr4:69082200-69082800	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr4:69082200-69084200	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr4:69082400-69082600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr4:69082400-69083000	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr4:69082800-69083200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr4:69083000-69083800	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr4:69083200-69083600	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr4:69083200-69084000	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr4:69083400-69084200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr4:69096800-69097200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr4:69099000-69099200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
26	chr4:69108000-69108400	Weak transcription	Esophagus	oesophagus
27	chr4:69108400-69108600	Enhancers	Esophagus	oesophagus
28	chr4:69109800-69115000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr4:69114800-69115000	Enhancers	GM12878-XiMat	blood
30	chr4:69115000-69115400	Flanking Active TSS	GM12878-XiMat	blood
31	chr4:69115000-69116200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr4:69115400-69115600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr4:69115400-69115800	Enhancers	GM12878-XiMat	blood
34	chr4:69115800-69116200	Enhancers	Placenta Amnion	Placenta Amnion
35	chr4:69116200-69116400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr4:69116200-69121600	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr4:69116200-69133200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr4:69121400-69121600	Enhancers	K562	blood
39	chr4:69121600-69121800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr4:69121600-69121800	Flanking Active TSS	K562	blood
41	chr4:69121600-69122200	Enhancers	Placenta Amnion	Placenta Amnion
42	chr4:69121800-69122000	Enhancers	K562	blood
43	chr4:69121800-69122200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr4:69122000-69122400	Flanking Active TSS	K562	blood
45	chr4:69122200-69122600	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr4:69122200-69122800	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr4:69122200-69125400	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr4:69122400-69122600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr4:69122400-69123000	Enhancers	K562	blood
50	chr4:69125200-69125800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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