Variant report

Variant	esv3325720
Chromosome Location	chr6:44094199-44096747
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:646)
CpG islands
(count:367)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:646 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:44094137-44094554	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:44094416-44094705	K562	blood:	n/a	n/a
3	ARID3A	chr6:44095062-44095155	HepG2	liver:	n/a	n/a
4	ATF2	chr6:44094334-44094861	GM12878	blood:	n/a	n/a
5	ATF3	chr6:44095004-44095253	K562	blood:	n/a	n/a
6	BACH1	chr6:44094684-44095234	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr6:44094419-44094779	GM12878	blood:	n/a	n/a
8	BCL3	chr6:44094909-44095272	GM12878	blood:	n/a	chr6:44095095-44095104
9	BHLHE40	chr6:44094576-44094816	K562	blood:	n/a	n/a
10	BHLHE40	chr6:44095075-44095180	GM12878	blood:	n/a	n/a
11	BHLHE40	chr6:44094355-44094807	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:44094671-44094845	HepG2	liver:	n/a	n/a
13	BHLHE40	chr6:44095945-44096223	K562	blood:	n/a	chr6:44095970-44095986
14	BHLHE40	chr6:44095140-44095222	K562	blood:	n/a	n/a
15	BRCA1	chr6:44095132-44095138	HepG2	liver:	n/a	n/a
16	BRCA1	chr6:44094978-44095127	GM12878	blood:	n/a	n/a
17	BRCA1	chr6:44094423-44094792	HepG2	liver:	n/a	n/a
18	CBX3	chr6:44096541-44096934	K562	blood:	n/a	n/a
19	CBX3	chr6:44094220-44094912	K562	blood:	n/a	n/a
20	CCNT2	chr6:44096325-44096435	K562	blood:	n/a	chr6:44096383-44096392
21	CCNT2	chr6:44094448-44096117	K562	blood:	n/a	chr6:44095812-44095821 chr6:44094697-44094706 chr6:44095686-44095695 chr6:44095692-44095701 chr6:44095344-44095353 chr6:44095356-44095365 chr6:44095653-44095662 chr6:44095575-44095584 chr6:44095350-44095359
22	CEBPB	chr6:44094494-44094817	K562	blood:	n/a	n/a
23	CEBPB	chr6:44094464-44094833	IMR90	lung:	n/a	n/a
24	CEBPD	chr6:44094969-44095270	HepG2	liver:	n/a	n/a
25	CEBPD	chr6:44095352-44095632	HepG2	liver:	n/a	n/a
26	CEBPD	chr6:44094978-44095216	HepG2	liver:	n/a	n/a
27	CHD1	chr6:44094288-44095216	GM12878	blood:	n/a	n/a
28	CHD1	chr6:44096008-44096051	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr6:44095047-44095273	HepG2	liver:	n/a	n/a
30	CHD2	chr6:44094965-44095474	K562	blood:	n/a	chr6:44095365-44095375
31	CHD2	chr6:44095011-44095563	GM12878	blood:	n/a	chr6:44095365-44095375
32	CHD2	chr6:44094431-44094787	GM12878	blood:	n/a	n/a
33	CHD2	chr6:44094491-44095666	Hela-S3	cervix:	n/a	chr6:44095365-44095375
34	CREB1	chr6:44095027-44095223	A549	lung:	n/a	n/a
35	CREB1	chr6:44095016-44095306	A549	lung:	n/a	n/a
36	CTCF	chr6:44096000-44096150	HA-sp	spinal cord:	n/a	n/a
37	CTCF	chr6:44094520-44094670	GM12871	blood:	n/a	n/a
38	CTCF	chr6:44096220-44096370	GM12864	blood:	n/a	n/a
39	CTCF	chr6:44096080-44096230	GM12875	blood:	n/a	n/a
40	CTCF	chr6:44096160-44096310	HAc	cerebellar:	n/a	n/a
41	CTCF	chr6:44096000-44096150	GM12864	blood:	n/a	n/a
42	CTCF	chr6:44096160-44096310	BE2_C	brain:	n/a	n/a
43	CTCF	chr6:44096060-44096210	HepG2	liver:	n/a	n/a
44	CTCF	chr6:44096040-44096190	HMF	breast:	n/a	n/a
45	CTCF	chr6:44096060-44096210	K562	blood:	n/a	n/a
46	CTCF	chr6:44094280-44094430	GM12871	blood:	n/a	n/a
47	CTCF	chr6:44096005-44096110	MCF-7	breast:	n/a	n/a
48	CTCF	chr6:44096020-44096170	GM12874	blood:	n/a	n/a
49	CTCF	chr6:44096228-44096431	HepG2	liver:	n/a	n/a
50	CTCF	chr6:44095980-44096130	HPAF	blood vessel:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:44096542-44096592	ovcar-3	ovarian:	n/a
2	chr6:44096542-44096592	ovcar-3	ovarian:	n/a
3	chr6:44095569-44095619	MCF10A-Er-Src	breast:	n/a
4	chr6:44095094-44095144	NH-A	brain:	n/a
5	chr6:44094852-44094902	SAEC	small airway:	n/a
6	chr6:44096081-44096131	MCF10A-Er-Src	breast:	n/a
7	chr6:44095108-44095158	Jurkat	blood:	n/a
8	chr6:44096081-44096131	RPTEC	kidney:	n/a
9	chr6:44094852-44094902	U87	brain:	n/a
10	chr6:44094852-44094902	LNCaP	prostate:	n/a
11	chr6:44095108-44095158	RPTEC	kidney:	n/a
12	chr6:44095094-44095144	LNCaP	prostate:	n/a
13	chr6:44096081-44096131	Jurkat	blood:	n/a
14	chr6:44096081-44096131	NH-A	brain:	n/a
15	chr6:44095569-44095619	GM19239	blood:	n/a
16	chr6:44095094-44095144	HCM	heart:	n/a
17	chr6:44094852-44094902	HL-60	blood:	n/a
18	chr6:44094852-44094902	BE2_C	brain:	n/a
19	chr6:44094852-44094902	HepG2	liver:	n/a
20	chr6:44094852-44094902	MCF10A-Er-Src	breast:	n/a
21	chr6:44095569-44095619	HCT-116	colon:	n/a
22	chr6:44095569-44095619	BJ	skin:	n/a
23	chr6:44095094-44095144	SAEC	small airway:	n/a
24	chr6:44095569-44095619	HRCEpiC	kidney:	n/a
25	chr6:44096542-44096592	SAEC	small airway:	n/a
26	chr6:44095569-44095619	HRE	kidney:	n/a
27	chr6:44095108-44095158	HEEpiC	esophagus:	n/a
28	chr6:44095108-44095158	HepG2	liver:	n/a
29	chr6:44095094-44095144	NHDF-neo	bronchial:	n/a
30	chr6:44094852-44094902	HCF	heart:	n/a
31	chr6:44096081-44096131	ovcar-3	ovarian:	n/a
32	chr6:44096081-44096131	H1-hESC	embryonic stem cell:	embryo
33	chr6:44094852-44094902	HCM	heart:	n/a
34	chr6:44094852-44094902	HUVEC	blood vessel:	n/a
35	chr6:44095094-44095144	PrEC	prostate:	n/a
36	chr6:44096542-44096592	AoSMC	blood vessel:	n/a
37	chr6:44095108-44095158	GM12892	blood:	n/a
38	chr6:44095569-44095619	NB4	blood:	n/a
39	chr6:44094852-44094902	GM06990	blood:	n/a
40	chr6:44095569-44095619	GM12891	blood:	n/a
41	chr6:44095094-44095144	SK-N-MC	brain:	n/a
42	chr6:44095569-44095619	MCF-7	breast:	n/a
43	chr6:44096081-44096131	AG04450	lung:	fetal
44	chr6:44096081-44096131	NB4	blood:	n/a
45	chr6:44096081-44096131	AG10803	skin:	n/a
46	chr6:44095569-44095619	HCM	heart:	n/a
47	chr6:44095094-44095144	HRPEpiC	eye:	n/a
48	chr6:44095094-44095144	A549	lung:	n/a
49	chr6:44095094-44095144	HPAEpiC	pulmonary alveolar:	n/a
50	chr6:44095569-44095619	T-47D	breast:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:43596367..43598855-chr6:44092530..44095404,4	K562	blood:
2	chr6:44093355..44096767-chr6:44213001..44216421,7	K562	blood:
3	chr11:62608617..62609721-chr6:44094675..44095678,3	NB4	blood:
4	chr1:171750621..171751192-chr6:44094734..44095532,2	Hela-S3	cervix:
5	chr6:43740232..43742498-chr6:44094487..44097613,3	K562	blood:
6	chr6:44094044..44095024-chr7:99214204..99214912,2	Hela-S3	cervix:
7	chr6:44095603..44096130-chr6:44224891..44225616,2	K562	blood:
8	chr6:44042031..44044413-chr6:44095279..44097168,2	K562	blood:
9	chr6:44093102..44095527-chr6:44231141..44233414,2	MCF-7	breast:
10	chr6:44095005..44097134-chr6:44184170..44186416,2	K562	blood:
11	chr6:43595621..43598855-chr6:44092842..44097752,6	K562	blood:
12	chr6:44093312..44099146-chr6:44212809..44220233,13	MCF-7	breast:
13	chr6:44095576..44096087-chr6:44119284..44120059,2	MCF-7	breast:
14	chr6:44042539..44044412-chr6:44091796..44094551,2	K562	blood:
15	chr6:44094685..44097058-chr6:44213813..44216236,2	MCF-7	breast:
16	chr6:44092682..44101478-chr6:44189085..44198306,11	K562	blood:
17	chr6:44093355..44100261-chr6:44212966..44217093,13	K562	blood:
18	chr6:44093370..44096253-chr6:44223564..44226835,7	K562	blood:
19	chr6:44055370..44058215-chr6:44094460..44096529,3	K562	blood:
20	chr6:44055370..44058215-chr6:44094927..44096529,2	K562	blood:
21	chr6:44094789..44096473-chr6:44279267..44282226,2	K562	blood:
22	chr6:44092343..44095710-chr6:44231665..44234902,4	K562	blood:
23	chr6:44094061..44096796-chr6:44223845..44226294,3	K562	blood:
24	chr6:44096398..44099100-chr6:44201010..44203822,2	K562	blood:

No data

Variant related genes	Relation type
TMEM63B	TF binding region
MRPL14	TF binding region
TMEM63B	CpG island
MRPL14	CpG island
ENSG00000112715	chromatin interactions
ENSG00000262179	chromatin interactions
ENSG00000146232	chromatin interactions
ENSG00000237686	chromatin interactions
ENSG00000183239	chromatin interactions
ENSG00000172432	chromatin interactions
ENSG00000157593	chromatin interactions
ENSG00000124688	chromatin interactions
ENSG00000112759	chromatin interactions
ENSG00000096384	chromatin interactions
ENSG00000124608	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000010165	chromatin interactions
ENSG00000197037	chromatin interactions

Extended variants
information (count: 68 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:68 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561086201	chr6:44094204-44094205	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs190820442	chr6:44094211-44094212	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs544159336	chr6:44094213-44094214	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs546816726	chr6:44094226-44094227	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs571489967	chr6:44094299-44094300	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs4714750	chr6:44094305-44094306	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs183086655	chr6:44094351-44094352	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs569495790	chr6:44094352-44094353	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs536691099	chr6:44094356-44094357	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs564387857	chr6:44094366-44094367	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs11419717	chr6:44094388-44094389	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs79920029	chr6:44094390-44094391	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs573808709	chr6:44094427-44094428	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs146661802	chr6:44094437-44094438	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs186535752	chr6:44094440-44094441	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs577784967	chr6:44094616-44094617	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
17	rs545141691	chr6:44094626-44094627	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs563443806	chr6:44094633-44094634	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs376456280	chr6:44094690-44094691	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
20	rs115366175	chr6:44094719-44094720	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
21	rs560922893	chr6:44094726-44094727	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
22	rs528594237	chr6:44094745-44094746	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
23	rs546703009	chr6:44094772-44094773	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
24	rs565350296	chr6:44094788-44094789	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
25	rs532608904	chr6:44094799-44094800	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
26	rs551146630	chr6:44094829-44094830	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
27	rs569501117	chr6:44094860-44094861	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
28	rs536931889	chr6:44094885-44094886	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
29	rs200026840	chr6:44094890-44094891	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
30	rs558838580	chr6:44094905-44094906	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
31	rs72348651	chr6:44094906-44094907	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
32	rs577201769	chr6:44094924-44094925	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
33	rs544480967	chr6:44094925-44094926	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
34	rs530577848	chr6:44094952-44094953	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
35	rs549033859	chr6:44095013-44095014	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
36	rs567286221	chr6:44095088-44095089	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
37	rs111763940	chr6:44095094-44095095	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
38	rs534573147	chr6:44095149-44095150	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
39	rs577194297	chr6:44095181-44095182	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
40	rs77423333	chr6:44095280-44095281	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
41	rs571279240	chr6:44095327-44095328	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
42	rs538496760	chr6:44095343-44095344	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
43	rs112750340	chr6:44095542-44095543	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
44	rs557115366	chr6:44095545-44095546	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
45	rs575476892	chr6:44095690-44095691	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
46	rs542495859	chr6:44095877-44095878	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
47	rs554406674	chr6:44095904-44095905	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs113463098	chr6:44095934-44095935	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs572922317	chr6:44095969-44095970	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs2096199	chr6:44096014-44096015	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:96)

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
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
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
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	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
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Colorectal cancer	16790693	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	19287148	CNVD
Colorectal cancer	19359472	CNVD
Multiple myeloma	16616336	CNVD
Chordoma	18071362	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	21569311	CNVD
Cancer	20164920	CNVD
lymphocytic leukemia	21291569	CNVD
Lung adenocarcinoma	17982442	CNVD

Chromatin state (count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44087400-44094200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
2	chr6:44089600-44094200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:44090400-44094200	Enhancers	Primary B cells from peripheral blood	blood
4	chr6:44090600-44094200	Enhancers	Small Intestine	intestine
5	chr6:44092200-44094200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr6:44092200-44094400	Transcr. at gene 5' and 3'	K562	blood
7	chr6:44092400-44094200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:44092600-44094400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr6:44092800-44094200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr6:44093000-44094200	Enhancers	Left Ventricle	heart
11	chr6:44093000-44094600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr6:44093200-44094200	Enhancers	Placenta	Placenta
13	chr6:44093200-44094400	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr6:44093200-44094600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr6:44093200-44096200	Active TSS	Lung	lung
16	chr6:44093400-44094400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
17	chr6:44093400-44094400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
18	chr6:44093400-44094400	Flanking Active TSS	Hela-S3	cervix
19	chr6:44093400-44094400	Flanking Active TSS	NHLF	lung
20	chr6:44093400-44094600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr6:44093400-44094600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr6:44093400-44094600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr6:44093400-44094600	Flanking Active TSS	Dnd41	blood
24	chr6:44093400-44096200	Active TSS	Breast Myoepithelial Primary Cells	Breast
25	chr6:44093600-44094200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
26	chr6:44093600-44094200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr6:44093600-44094200	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr6:44093600-44094200	Transcr. at gene 5' and 3'	HUES48 Cell Line	embryonic stem cell
29	chr6:44093600-44094200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
30	chr6:44093600-44094200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr6:44093600-44094200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr6:44093600-44094200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr6:44093600-44094200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
34	chr6:44093600-44094200	Flanking Active TSS	Fetal Intestine Small	intestine
35	chr6:44093600-44094200	Flanking Active TSS	Fetal Kidney	kidney
36	chr6:44093600-44094200	Enhancers	Spleen	Spleen
37	chr6:44093600-44094200	Flanking Bivalent TSS/Enh	HepG2	liver
38	chr6:44093600-44094200	Flanking Active TSS	HSMM	muscle
39	chr6:44093600-44094200	Flanking Active TSS	NHDF-Ad	bronchial
40	chr6:44093600-44094200	Flanking Active TSS	Osteobl	bone
41	chr6:44093600-44094400	Flanking Active TSS	H1 Cell Line	embryonic stem cell
42	chr6:44093600-44094400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr6:44093600-44094400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
44	chr6:44093600-44094400	Flanking Active TSS	Primary T cells from cord blood	blood
45	chr6:44093600-44094400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
46	chr6:44093600-44094400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr6:44093600-44094400	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
48	chr6:44093600-44094400	Flanking Active TSS	Fetal Lung	lung
49	chr6:44093600-44094400	Flanking Active TSS	Fetal Muscle Leg	muscle
50	chr6:44093600-44094400	Enhancers	Gastric	stomach

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