Variant report

Variant	esv1811041
Chromosome Location	chr6:34851134-34856501
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:566)
CpG islands
(count:918)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:566 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:34855719-34856923	K562	blood:	n/a	n/a
2	ATF1	chr6:34855487-34856397	K562	blood:	n/a	chr6:34855838-34855852
3	ATF2	chr6:34855474-34856393	H1-hESC	embryonic stem cell:	n/a	chr6:34855838-34855852
4	ATF2	chr6:34855528-34856206	GM12878	blood:	n/a	chr6:34855838-34855852
5	ATF2	chr6:34855555-34856110	GM12878	blood:	n/a	chr6:34855838-34855852
6	ATF2	chr6:34855549-34856136	H1-hESC	embryonic stem cell:	n/a	chr6:34855838-34855852
7	ATF3	chr6:34855748-34855947	GM12878	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
8	ATF3	chr6:34855564-34856045	K562	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
9	ATF3	chr6:34855584-34856143	HepG2	liver:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
10	ATF3	chr6:34855553-34856043	K562	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
11	ATF3	chr6:34855626-34856017	H1-hESC	embryonic stem cell:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
12	ATF3	chr6:34855565-34856126	K562	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
13	ATF3	chr6:34855569-34856012	HepG2	liver:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
14	ATF3	chr6:34855595-34856148	GM12878	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
15	ATF3	chr6:34855611-34856089	A549	lung:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
16	ATF3	chr6:34855575-34856023	H1-hESC	embryonic stem cell:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
17	BCL3	chr6:34855610-34855991	GM12878	blood:	n/a	n/a
18	BCLAF1	chr6:34855498-34856151	GM12878	blood:	n/a	n/a
19	BCLAF1	chr6:34855583-34856152	GM12878	blood:	n/a	n/a
20	BHLHE40	chr6:34855612-34856038	GM12878	blood:	n/a	n/a
21	BHLHE40	chr6:34855593-34856100	K562	blood:	n/a	n/a
22	BRCA1	chr6:34855671-34856036	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr6:34855787-34856109	GM12878	blood:	n/a	n/a
24	BRCA1	chr6:34855630-34856250	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr6:34855662-34856196	HepG2	liver:	n/a	n/a
26	CBX3	chr6:34855652-34856179	K562	blood:	n/a	n/a
27	CBX3	chr6:34855492-34857137	K562	blood:	n/a	n/a
28	CCNT2	chr6:34855577-34856270	K562	blood:	n/a	n/a
29	CEBPB	chr6:34855604-34856267	K562	blood:	n/a	n/a
30	CEBPB	chr6:34855470-34856309	GM12878	blood:	n/a	n/a
31	CEBPB	chr6:34853686-34853985	K562	blood:	n/a	n/a
32	CEBPB	chr6:34853734-34853964	K562	blood:	n/a	n/a
33	CEBPB	chr6:34855573-34856151	K562	blood:	n/a	n/a
34	CEBPB	chr6:34855691-34856203	HepG2	liver:	n/a	n/a
35	CEBPD	chr6:34855485-34856206	K562	blood:	n/a	n/a
36	CEBPD	chr6:34855573-34856031	HepG2	liver:	n/a	n/a
37	CHD1	chr6:34855161-34855323	GM12878	blood:	n/a	n/a
38	CHD1	chr6:34855533-34856594	GM12878	blood:	n/a	n/a
39	CHD1	chr6:34855352-34856900	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr6:34855559-34856008	GM12878	blood:	n/a	n/a
41	CHD2	chr6:34855549-34856172	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr6:34855433-34856316	K562	blood:	n/a	n/a
43	CHD2	chr6:34855618-34856113	HepG2	liver:	n/a	n/a
44	CHD2	chr6:34855656-34857154	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr6:34855374-34856571	GM12878	blood:	n/a	chr6:34855839-34855852
46	CREB1	chr6:34855354-34856195	ECC-1	luminal epithelium:	n/a	chr6:34855839-34855852
47	CREB1	chr6:34856455-34857463	K562	blood:	n/a	n/a
48	CREB1	chr6:34855279-34856399	HepG2	liver:	n/a	chr6:34855839-34855852
49	CREB1	chr6:34855202-34856440	HepG2	liver:	n/a	chr6:34855839-34855852
50	CREB1	chr6:34856421-34857758	HepG2	liver:	n/a	n/a

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34855635-34855685	AG10803	skin:	n/a
2	chr6:34856217-34856267	BE2_C	brain:	n/a
3	chr6:34853620-34853670	GM12878	blood:	n/a
4	chr6:34855635-34855685	AG10803	skin:	n/a
5	chr6:34856217-34856267	BE2_C	brain:	n/a
6	chr6:34853620-34853670	GM12878	blood:	n/a
7	chr6:34853620-34853670	HepG2	liver:	n/a
8	chr6:34855797-34855847	HRCEpiC	kidney:	n/a
9	chr6:34855834-34855884	AoSMC	blood vessel:	n/a
10	chr6:34855885-34855935	AG10803	skin:	n/a
11	chr6:34855885-34855935	ProgFib	skin:	n/a
12	chr6:34855797-34855847	HepG2	liver:	n/a
13	chr6:34855980-34856030	SK-N-SH_RA	brain:	n/a
14	chr6:34856158-34856208	SKMC	muscle:	n/a
15	chr6:34855635-34855685	NB4	blood:	n/a
16	chr6:34855797-34855847	SK-N-MC	brain:	n/a
17	chr6:34855980-34856030	NHBE	bronchial:	n/a
18	chr6:34855980-34856030	NT2-D1	testis:	n/a
19	chr6:34853620-34853670	U87	brain:	n/a
20	chr6:34855839-34855889	ECC-1	luminal epithelium:	n/a
21	chr6:34855635-34855685	NHBE	bronchial:	n/a
22	chr6:34856217-34856267	AoSMC	blood vessel:	n/a
23	chr6:34855885-34855935	AG09319	gingival:	n/a
24	chr6:34855789-34855839	AG09319	gingival:	n/a
25	chr6:34853620-34853670	HCM	heart:	n/a
26	chr6:34855980-34856030	HIPEpiC	eye:	n/a
27	chr6:34855980-34856030	HPAEpiC	pulmonary alveolar:	n/a
28	chr6:34855408-34855458	HRE	kidney:	n/a
29	chr6:34852903-34852953	SAEC	small airway:	n/a
30	chr6:34855797-34855847	AG09309	skin:	n/a
31	chr6:34855470-34855520	HepG2	liver:	n/a
32	chr6:34855797-34855847	HIPEpiC	eye:	n/a
33	chr6:34855980-34856030	AG09309	skin:	n/a
34	chr6:34853620-34853670	H1-hESC	embryonic stem cell:	embryo
35	chr6:34855885-34855935	GM06990	blood:	n/a
36	chr6:34853620-34853670	HCT-116	colon:	n/a
37	chr6:34855635-34855685	Jurkat	blood:	n/a
38	chr6:34855408-34855458	HepG2	liver:	n/a
39	chr6:34855797-34855847	LNCaP	prostate:	n/a
40	chr6:34856217-34856267	GM06990	blood:	n/a
41	chr6:34855408-34855458	HEEpiC	esophagus:	n/a
42	chr6:34855789-34855839	HCPEpiC	choroid plexus:	n/a
43	chr6:34856135-34856185	K562	blood:	n/a
44	chr6:34856135-34856185	AG10803	skin:	n/a
45	chr6:34855887-34855937	AG09309	skin:	n/a
46	chr6:34855797-34855847	HL-60	blood:	n/a
47	chr6:34855834-34855884	HCPEpiC	choroid plexus:	n/a
48	chr6:34855470-34855520	LNCaP	prostate:	n/a
49	chr6:34855980-34856030	SAEC	small airway:	n/a
50	chr6:34855980-34856030	HepG2	liver:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:2419677..2420373-chr6:34855480..34855994,2	Hela-S3	cervix:
2	chr3:156534879..156535549-chr6:34855191..34855795,2	Hela-S3	cervix:
3	chr6:34843479..34847323-chr6:34849401..34853884,4	MCF-7	breast:
4	chr6:34392840..34394590-chr6:34855825..34858514,2	K562	blood:
5	chr6:34834250..34837156-chr6:34851105..34853013,3	MCF-7	breast:
6	chr6:27798350..27799895-chr6:34855095..34857385,2	K562	blood:
7	chr6:34856224..34858095-chr6:35226235..35229197,2	MCF-7	breast:
8	chr6:34853391..34855742-chr6:34918404..34920858,2	K562	blood:
9	chr17:73285374..73286157-chr6:34855342..34855976,2	Hela-S3	cervix:
10	chr12:120729250..120730043-chr6:34855337..34856229,2	Hela-S3	cervix:
11	chr15:41913003..41913826-chr6:34855469..34856066,2	Hela-S3	cervix:
12	chr17:56708594..56709416-chr6:34855776..34856394,2	Hela-S3	cervix:
13	chr6:34758735..34762506-chr6:34853024..34858695,7	MCF-7	breast:
14	chr6:34855693..34857942-chr6:35191744..35194149,2	MCF-7	breast:
15	chr6:34855314..34856910-chr6:35435686..35437650,2	MCF-7	breast:
16	chr6:34842945..34852488-chr6:34852501..34858927,16	MCF-7	breast:
17	chr6:34759044..34761297-chr6:34854138..34856970,2	K562	blood:
18	chr6:34837346..34838981-chr6:34850648..34853394,2	K562	blood:
19	chr6:34853107..34854715-chr6:34857316..34859285,2	MCF-7	breast:
20	chr6:34733163..34735637-chr6:34853537..34855573,2	K562	blood:
21	chr6:34723520..34726444-chr6:34854512..34857469,3	MCF-7	breast:
22	chr6:34854986..34858344-chr6:35226281..35229493,3	K562	blood:

No data

Variant related genes	Relation type
ANKS1A	TF binding region
TAF11	TF binding region
ANKS1A	CpG island
TAF11	CpG island
ENSG00000202538	chromatin interactions
ENSG00000064999	chromatin interactions
ENSG00000272374	chromatin interactions
ENSG00000270800	chromatin interactions
ENSG00000159733	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000125454	chromatin interactions
ENSG00000197914	chromatin interactions
ENSG00000065029	chromatin interactions
ENSG00000198755	chromatin interactions
ENSG00000124562	chromatin interactions
ENSG00000064995	chromatin interactions
ENSG00000124614	chromatin interactions
ENSG00000174197	chromatin interactions
ENSG00000065060	chromatin interactions

Extended variants
information (count: 218 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:218 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2273006	chr6:34851134-34851135	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs74696211	chr6:34851141-34851142	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs202137157	chr6:34851153-34851154	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs548605305	chr6:34851158-34851159	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs551833041	chr6:34851159-34851160	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs13198340	chr6:34851211-34851212	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs188620142	chr6:34851216-34851217	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs181046361	chr6:34851249-34851250	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs530221346	chr6:34851258-34851259	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs77487017	chr6:34851337-34851338	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs115434816	chr6:34851355-34851356	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs561446015	chr6:34851375-34851376	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs34105271	chr6:34851398-34851399	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs150175475	chr6:34851446-34851447	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs185912914	chr6:34851467-34851468	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs140157873	chr6:34851473-34851474	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs143889919	chr6:34851512-34851513	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs189103116	chr6:34851539-34851540	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs116921367	chr6:34851558-34851559	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs539039074	chr6:34851579-34851580	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs145837877	chr6:34851584-34851585	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs34009883	chr6:34851589-34851590	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs148975395	chr6:34851668-34851669	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs79913660	chr6:34851683-34851684	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs181550254	chr6:34851777-34851778	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs561818713	chr6:34851778-34851779	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs76601069	chr6:34851784-34851785	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs74510225	chr6:34851800-34851801	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs76168382	chr6:34851822-34851823	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs35960327	chr6:34851851-34851852	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs574995385	chr6:34851883-34851884	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs542381175	chr6:34851925-34851926	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs563752006	chr6:34851976-34851977	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs530964473	chr6:34852002-34852003	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs552255068	chr6:34852113-34852114	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs35035833	chr6:34852127-34852128	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs4646930	chr6:34852150-34852151	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs528735343	chr6:34852152-34852153	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs547183009	chr6:34852159-34852160	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs187590432	chr6:34852167-34852168	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs4646929	chr6:34852176-34852177	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs4646928	chr6:34852177-34852178	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs537229891	chr6:34852185-34852186	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs550286770	chr6:34852194-34852195	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs568593719	chr6:34852211-34852212	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs4646927	chr6:34852217-34852218	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs151159731	chr6:34852234-34852235	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs182912297	chr6:34852236-34852237	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs4646926	chr6:34852253-34852254	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs539130314	chr6:34852260-34852261	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD

Chromatin state (count:505 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34816800-34853600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:34817400-34851200	Strong transcription	Fetal Thymus	thymus
3	chr6:34818600-34853400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr6:34820200-34855000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr6:34821000-34854600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:34823000-34851600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr6:34830000-34855000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr6:34834400-34851200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr6:34834400-34853600	Strong transcription	Primary T helper cells fromperipheralblood	blood
10	chr6:34835800-34855200	Weak transcription	Small Intestine	intestine
11	chr6:34837000-34852000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr6:34837000-34852400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
13	chr6:34837400-34851200	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr6:34838800-34851200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr6:34840600-34851200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr6:34840800-34854800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:34841400-34854600	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr6:34841400-34855200	Weak transcription	Fetal Heart	heart
19	chr6:34841600-34854600	Weak transcription	Fetal Kidney	kidney
20	chr6:34842600-34854800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr6:34844000-34854000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr6:34844000-34854800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr6:34844600-34853400	Strong transcription	HUES64 Cell Line	embryonic stem cell
24	chr6:34844600-34854600	Weak transcription	Psoas Muscle	Psoas
25	chr6:34845000-34854600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr6:34845200-34853800	Weak transcription	Fetal Brain Male	brain
27	chr6:34845400-34854600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr6:34845600-34851200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr6:34845600-34852200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr6:34846600-34854600	Weak transcription	HMEC	breast
31	chr6:34847600-34854600	Weak transcription	Right Ventricle	heart
32	chr6:34848000-34853600	Weak transcription	Fetal Brain Female	brain
33	chr6:34848000-34854400	Weak transcription	Stomach Smooth Muscle	stomach
34	chr6:34848000-34854600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr6:34848000-34854600	Weak transcription	Brain Germinal Matrix	brain
36	chr6:34848000-34854600	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr6:34848000-34854600	Weak transcription	Thymus	Thymus
38	chr6:34848000-34854600	Weak transcription	HSMMtube	muscle
39	chr6:34848000-34854600	Weak transcription	NHLF	lung
40	chr6:34848000-34854800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr6:34848000-34854800	Weak transcription	Gastric	stomach
42	chr6:34848200-34853400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr6:34848200-34853400	Weak transcription	Pancreas	Pancrea
44	chr6:34848200-34854000	Weak transcription	Fetal Muscle Leg	muscle
45	chr6:34848200-34854000	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr6:34848200-34854000	Weak transcription	NHEK	skin
47	chr6:34848200-34854400	Weak transcription	Colonic Mucosa	Colon
48	chr6:34848200-34854600	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr6:34848200-34854600	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr6:34848200-34854600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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