Variant report

Variant	esv3384876
Chromosome Location	chr6:146055559-146057657
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:773)
CpG islands
(count:367)
Chromatin interactive
region (count:23)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:773 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:146055459-146056158	K562	blood:	n/a	n/a
2	ARID3A	chr6:146057198-146057248	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:146055703-146056408	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:146056640-146056950	HepG2	liver:	n/a	n/a
5	ATF2	chr6:146055583-146056126	GM12878	blood:	n/a	n/a
6	ATF2	chr6:146056722-146057541	GM12878	blood:	n/a	n/a
7	ATF2	chr6:146055700-146056255	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr6:146055751-146056303	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr6:146056839-146057271	GM12878	blood:	n/a	n/a
10	BACH1	chr6:146056742-146057090	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr6:146055950-146056520	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCLAF1	chr6:146055584-146057472	GM12878	blood:	n/a	chr6:146056929-146056938 chr6:146056638-146056651 chr6:146056681-146056694 chr6:146055898-146055911 chr6:146056643-146056652 chr6:146056085-146056098 chr6:146056635-146056648 chr6:146056640-146056649
13	BCLAF1	chr6:146055626-146057292	K562	blood:	n/a	chr6:146056929-146056938 chr6:146056638-146056651 chr6:146056681-146056694 chr6:146055898-146055911 chr6:146056643-146056652 chr6:146056085-146056098 chr6:146056635-146056648 chr6:146056640-146056649
14	BCLAF1	chr6:146056511-146057323	GM12878	blood:	n/a	chr6:146056929-146056938 chr6:146056638-146056651 chr6:146056681-146056694 chr6:146056643-146056652 chr6:146056635-146056648 chr6:146056640-146056649
15	BCLAF1	chr6:146055709-146056329	GM12878	blood:	n/a	chr6:146055898-146055911 chr6:146056085-146056098
16	BHLHE40	chr6:146056682-146057034	A549	lung:	n/a	n/a
17	BHLHE40	chr6:146055796-146057399	K562	blood:	n/a	chr6:146056676-146056692
18	BHLHE40	chr6:146055480-146057455	GM12878	blood:	n/a	chr6:146056676-146056692
19	BHLHE40	chr6:146055762-146057226	HepG2	liver:	n/a	chr6:146056676-146056692
20	BRCA1	chr6:146055875-146056062	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr6:146055627-146056142	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr6:146056878-146057138	GM12878	blood:	n/a	n/a
23	BRCA1	chr6:146055847-146056407	HepG2	liver:	n/a	n/a
24	CBX3	chr6:146056547-146057279	K562	blood:	n/a	n/a
25	CBX3	chr6:146055627-146056522	K562	blood:	n/a	n/a
26	CCNT2	chr6:146055680-146057243	K562	blood:	n/a	n/a
27	CEBPB	chr6:146056664-146057343	K562	blood:	n/a	n/a
28	CEBPB	chr6:146056919-146057280	A549	lung:	n/a	n/a
29	CEBPB	chr6:146055884-146057293	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr6:146057008-146057150	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr6:146056880-146057388	K562	blood:	n/a	n/a
32	CEBPB	chr6:146055891-146056118	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPD	chr6:146055702-146056201	HepG2	liver:	n/a	n/a
34	CEBPD	chr6:146055767-146056564	K562	blood:	n/a	n/a
35	CEBPD	chr6:146055689-146056733	HepG2	liver:	n/a	n/a
36	CEBPD	chr6:146056385-146056653	HepG2	liver:	n/a	n/a
37	CEBPD	chr6:146056760-146057068	HepG2	liver:	n/a	n/a
38	CHD1	chr6:146055551-146057403	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD1	chr6:146055655-146057464	GM12878	blood:	n/a	n/a
40	CHD2	chr6:146055750-146056422	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr6:146055894-146057056	K562	blood:	n/a	n/a
42	CHD2	chr6:146056634-146057184	GM12878	blood:	n/a	n/a
43	CHD2	chr6:146055851-146056062	GM12878	blood:	n/a	n/a
44	CHD2	chr6:146055827-146057137	HepG2	liver:	n/a	n/a
45	CHD2	chr6:146055782-146057275	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr6:146056655-146056970	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr6:146055578-146057392	K562	blood:	n/a	n/a
48	CREB1	chr6:146055654-146057365	HepG2	liver:	n/a	n/a
49	CREB1	chr6:146055702-146056885	A549	lung:	n/a	n/a
50	CREB1	chr6:146055823-146057422	GM12878	blood:	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	chr6:146056770-146056820	AG04450	lung:	fetal
2	chr6:146056770-146056820	AG04450	lung:	fetal
3	chr6:146056770-146056820	HMEC	breast:	n/a
4	chr6:146057055-146057105	AG10803	skin:	n/a
5	chr6:146056083-146056133	HRE	kidney:	n/a
6	chr6:146056083-146056133	BJ	skin:	n/a
7	chr6:146056083-146056133	GM19239	blood:	n/a
8	chr6:146056793-146056843	AG04450	lung:	fetal
9	chr6:146056083-146056133	PrEC	prostate:	n/a
10	chr6:146056083-146056133	HAEpiC	amniotic membrane:	n/a
11	chr6:146056793-146056843	HMEC	breast:	n/a
12	chr6:146056793-146056843	ECC-1	luminal epithelium:	n/a
13	chr6:146056083-146056133	Caco-2	colon:	n/a
14	chr6:146056770-146056820	PANC-1	pancreas:	n/a
15	chr6:146057073-146057123	AoSMC	blood vessel:	n/a
16	chr6:146056793-146056843	HL-60	blood:	n/a
17	chr6:146057055-146057105	SK-N-MC	brain:	n/a
18	chr6:146056419-146056469	HCM	heart:	n/a
19	chr6:146056770-146056820	HEEpiC	esophagus:	n/a
20	chr6:146056793-146056843	SKMC	muscle:	n/a
21	chr6:146056793-146056843	HNPCEpiC	eye:	n/a
22	chr6:146056793-146056843	BE2_C	brain:	n/a
23	chr6:146056793-146056843	NH-A	brain:	n/a
24	chr6:146056793-146056843	HUVEC	blood vessel:	n/a
25	chr6:146057073-146057123	H1-hESC	embryonic stem cell:	embryo
26	chr6:146057073-146057123	IMR90	lung:	fetal
27	chr6:146056793-146056843	SK-N-SH_RA	brain:	n/a
28	chr6:146056770-146056820	GM12878	blood:	n/a
29	chr6:146056770-146056820	HRPEpiC	eye:	n/a
30	chr6:146056419-146056469	MCF10A-Er-Src	breast:	n/a
31	chr6:146057073-146057123	Caco-2	colon:	n/a
32	chr6:146057055-146057105	AoSMC	blood vessel:	n/a
33	chr6:146056793-146056843	U87	brain:	n/a
34	chr6:146056793-146056843	HepG2	liver:	n/a
35	chr6:146056419-146056469	NH-A	brain:	n/a
36	chr6:146057055-146057105	HMEC	breast:	n/a
37	chr6:146056793-146056843	H1-hESC	embryonic stem cell:	embryo
38	chr6:146056083-146056133	NB4	blood:	n/a
39	chr6:146056770-146056820	HPAEpiC	pulmonary alveolar:	n/a
40	chr6:146057073-146057123	GM06990	blood:	n/a
41	chr6:146056770-146056820	NH-A	brain:	n/a
42	chr6:146057055-146057105	T-47D	breast:	n/a
43	chr6:146056419-146056469	GM12892	blood:	n/a
44	chr6:146056770-146056820	AoSMC	blood vessel:	n/a
45	chr6:146056083-146056133	IMR90	lung:	fetal
46	chr6:146056793-146056843	HEK293	kidney:	embryo
47	chr6:146057055-146057105	GM12892	blood:	n/a
48	chr6:146057073-146057123	NHDF-neo	bronchial:	n/a
49	chr6:146056793-146056843	HEEpiC	esophagus:	n/a
50	chr6:146056770-146056820	HL-60	blood:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:146052168..146062191-chr6:146124046..146141258,59	K562	blood:
2	chr19:55770065..55771348-chr6:146056333..146057332,3	Hela-S3	cervix:
3	chr1:110950353..110950869-chr6:146056622..146057613,2	Hela-S3	cervix:
4	chr12:44199788..44200535-chr6:146055682..146056650,2	Hela-S3	cervix:
5	chr1:228327693..228328321-chr6:146055580..146056537,2	Hela-S3	cervix:
6	chr6:146023773..146025394-chr6:146054656..146056157,2	K562	blood:
7	chr6:146047378..146061811-chr6:146118130..146137627,77	K562	blood:
8	chr6:146056240..146056988-chr7:100424823..100425448,2	HCT-116	colon:
9	chr19:16770512..16771052-chr6:146055843..146056790,2	Hela-S3	cervix:
10	chr6:146054881..146058754-chr6:146284576..146286666,3	K562	blood:
11	chr6:146056051..146056947-chr9:33025138..33025814,2	Hela-S3	cervix:
12	chr6:43595203..43596723-chr6:146055866..146057723,2	MCF-7	breast:
13	chr6:146054764..146058281-chr6:146133205..146137397,13	MCF-7	breast:
14	chr6:146055478..146057329-chr6:146213622..146216410,2	K562	blood:
15	chr6:146055814..146058166-chr6:146135376..146138309,3	MCF-7	breast:
16	chr11:62608720..62609583-chr6:146056117..146056835,2	NB4	blood:
17	chr6:146054743..146057884-chr6:146276241..146279001,3	K562	blood:
18	chr6:146055972..146056545-chr6:146135397..146135982,2	MCF-7	breast:
19	chr6:146051601..146058492-chr6:146282422..146286666,8	K562	blood:
20	chr10:75012200..75012758-chr6:146055684..146056249,2	Hela-S3	cervix:
21	chr6:146054188..146056153-chr6:146627133..146629580,2	K562	blood:
22	chr2:38977833..38978509-chr6:146055931..146056536,2	Hela-S3	cervix:
23	chr13:98794348..98794868-chr6:146056065..146056713,2	HCT-116	colon:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRM1-11	chr6:146056706-146058354	ENSG00000270638.1
2	lnc-GRM1-1	chr6:146056005-146056056	NONHSAT115397

No data

Variant related genes	Relation type
ENSG00000270638	TF binding region
EPM2A	TF binding region
ENSG00000270638	CpG island
EPM2A	CpG island
ENSG00000172432	chromatin interactions
ENSG00000268790	chromatin interactions
ENSG00000214046	chromatin interactions
ENSG00000196411	chromatin interactions
ENSG00000143774	chromatin interactions
ENSG00000134248	chromatin interactions
ENSG00000086061	chromatin interactions
ENSG00000137074	chromatin interactions
ENSG00000115875	chromatin interactions
ENSG00000151239	chromatin interactions
ENSG00000224699	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000182180	chromatin interactions
ENSG00000118496	chromatin interactions
ENSG00000152767	chromatin interactions
ENSG00000227540	chromatin interactions
ENSG00000105063	chromatin interactions
ENSG00000146414	chromatin interactions
ENSG00000235652	chromatin interactions

Extended variants
information (count: 91 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:91 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554346942	chr6:146055567-146055568	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs373233833	chr6:146055568-146055569	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs540085265	chr6:146055583-146055584	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs192752466	chr6:146055584-146055585	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs369251961	chr6:146055626-146055627	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs542626230	chr6:146055682-146055683	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs571377483	chr6:146055714-146055715	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs372607804	chr6:146055737-146055738	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs531669722	chr6:146055743-146055744	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs545487120	chr6:146055766-146055767	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs183144715	chr6:146055769-146055770	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs17798189	chr6:146055780-146055781	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs146479205	chr6:146055781-146055782	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs554687787	chr6:146055791-146055792	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs534023852	chr6:146055818-146055819	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs530447045	chr6:146055819-146055820	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs548668238	chr6:146055852-146055853	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs568844696	chr6:146055892-146055893	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
19	rs537499867	chr6:146055904-146055905	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
20	rs76383329	chr6:146055926-146055927	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
21	rs80292977	chr6:146055932-146055933	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
22	rs533713647	chr6:146055937-146055938	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
23	rs118049119	chr6:146055960-146055961	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
24	rs573561339	chr6:146055963-146055964	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
25	rs574024731	chr6:146055979-146055980	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
26	rs536547647	chr6:146055982-146055983	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
27	rs371086805	chr6:146055989-146055990	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
28	rs17798207	chr6:146056009-146056010	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs371627047	chr6:146056016-146056017	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
30	rs576381834	chr6:146056020-146056021	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
31	rs375070310	chr6:146056088-146056089	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
32	rs545112548	chr6:146056101-146056102	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
33	rs565361309	chr6:146056107-146056108	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
34	rs572601101	chr6:146056124-146056125	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
35	rs541610476	chr6:146056128-146056129	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
36	rs376977466	chr6:146056162-146056163	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
37	rs560099488	chr6:146056238-146056239	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
38	rs561483716	chr6:146056311-146056312	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
39	rs199544789	chr6:146056355-146056356	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
40	rs370423440	chr6:146056356-146056357	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
41	rs374826256	chr6:146056400-146056401	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
42	rs550455609	chr6:146056427-146056428	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
43	rs200673517	chr6:146056447-146056448	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
44	rs201510569	chr6:146056451-146056452	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
45	rs563875151	chr6:146056454-146056455	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
46	rs531330673	chr6:146056464-146056465	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
47	rs187930476	chr6:146056472-146056473	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
48	rs2235482	chr6:146056476-146056477	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs374338349	chr6:146056499-146056500	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
50	rs547147183	chr6:146056506-146056507	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Autism	22495311	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
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
lymphocytic leukemia	21291569	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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:146026800-146055800	Weak transcription	Left Ventricle	heart
2	chr6:146050400-146055600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr6:146050600-146055800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr6:146051000-146055600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr6:146052800-146055600	Weak transcription	Aorta	Aorta
6	chr6:146052800-146055600	Weak transcription	Ovary	ovary
7	chr6:146052800-146055800	Weak transcription	Gastric	stomach
8	chr6:146054200-146055800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr6:146054200-146055800	Weak transcription	Esophagus	oesophagus
10	chr6:146054800-146055600	Flanking Active TSS	Primary T cells from cord blood	blood
11	chr6:146054800-146055600	Flanking Active TSS	Dnd41	blood
12	chr6:146054800-146056200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr6:146054800-146057800	Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr6:146054800-146058400	Active TSS	Stomach Smooth Muscle	stomach
15	chr6:146055000-146055600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr6:146055000-146055600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr6:146055000-146055600	Enhancers	Primary B cells from peripheral blood	blood
18	chr6:146055000-146055600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr6:146055000-146055600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr6:146055000-146055600	Enhancers	Primary T helper cells fromperipheralblood	blood
21	chr6:146055000-146055600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr6:146055000-146055600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr6:146055000-146055600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
24	chr6:146055000-146055600	Flanking Active TSS	Brain Hippocampus Middle	brain
25	chr6:146055000-146055600	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
26	chr6:146055000-146055600	Flanking Active TSS	Fetal Brain Male	brain
27	chr6:146055000-146055600	Flanking Active TSS	A549	lung
28	chr6:146055000-146055800	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr6:146055000-146055800	Flanking Active TSS	Primary hematopoietic stem cells	blood
30	chr6:146055000-146055800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
31	chr6:146055000-146055800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
32	chr6:146055000-146056000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr6:146055000-146057200	Active TSS	HUES48 Cell Line	embryonic stem cell
34	chr6:146055000-146057200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr6:146055000-146057400	Active TSS	Right Ventricle	heart
36	chr6:146055000-146057600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:146055000-146057600	Active TSS	Colon Smooth Muscle	Colon
38	chr6:146055000-146057800	Active TSS	Brain Angular Gyrus	brain
39	chr6:146055000-146058000	Active TSS	Fetal Stomach	stomach
40	chr6:146055000-146058000	Active TSS	Thymus	Thymus
41	chr6:146055000-146058400	Active TSS	Brain Germinal Matrix	brain
42	chr6:146055000-146058400	Active TSS	Right Atrium	heart
43	chr6:146055200-146055600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr6:146055200-146055600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
45	chr6:146055200-146055600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr6:146055200-146055600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr6:146055200-146055600	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr6:146055200-146055600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chr6:146055200-146055600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
50	chr6:146055200-146055600	Flanking Active TSS	Adipose Nuclei	Adipose

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