Variant report

Variant	nsv437481
Chromosome Location	chr6:27655096-27683572
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:82)
LncRNA
region (count:36)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:82 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:27658926..27663446-chr6:27685398..27690588,6	K562	blood:
2	chr6:27657772..27659329-chr6:27759649..27761328,2	K562	blood:
3	chr6:27655564..27658376-chr6:27856463..27858379,2	K562	blood:
4	chr6:27677806..27681371-chr6:27682071..27685052,3	K562	blood:
5	chr6:27661665..27662337-chr6:27720402..27720938,2	MCF-7	breast:
6	chr6:27651230..27653525-chr6:27660393..27663354,2	MCF-7	breast:
7	chr6:27651170..27656145-chr6:27660253..27663653,4	MCF-7	breast:
8	chr6:27179126..27181346-chr6:27660529..27662958,2	K562	blood:
9	chr6:27661813..27662703-chr6:27719579..27720188,2	MCF-7	breast:
10	chr6:27676712..27678626-chr6:27679096..27681049,2	K562	blood:
11	chr6:27661606..27663243-chr6:27719625..27721150,2	K562	blood:
12	chr6:27635489..27641593-chr6:27648456..27655439,10	K562	blood:
13	chr6:27518096..27521091-chr6:27655240..27657826,2	K562	blood:
14	chr6:27260766..27263711-chr6:27659606..27661608,2	K562	blood:
15	chr6:27662005..27662637-chr6:31619681..31620477,2	Hela-S3	cervix:
16	chr6:27652290..27655444-chr6:27857919..27861967,3	K562	blood:
17	chr6:27676729..27679149-chr6:27683111..27685492,2	K562	blood:
18	chr6:27590776..27592562-chr6:27661680..27663552,2	MCF-7	breast:
19	chr6:27659790..27663314-chr6:27665578..27668905,6	K562	blood:
20	chr6:27652463..27655224-chr6:27720018..27721922,3	K562	blood:
21	chr6:27653789..27659338-chr6:27659392..27663401,13	K562	blood:
22	chr6:27655786..27657671-chr6:27777694..27780064,2	K562	blood:
23	chr6:27661331..27663089-chr6:27665763..27668347,2	K562	blood:
24	chr6:27526508..27528799-chr6:27655486..27657530,2	K562	blood:
25	chr6:27661478..27663340-chr6:27680780..27682655,2	K562	blood:
26	chr6:27661478..27663340-chr6:27680780..27682655,2	K562	blood:
27	chr6:27598632..27599274-chr6:27655396..27655916,2	K562	blood:
28	chr6:27676729..27679149-chr6:27683111..27685492,2	K562	blood:
29	chr6:27655233..27656837-chr6:27693147..27694855,2	K562	blood:
30	chr6:27100391..27103275-chr6:27661781..27664479,3	K562	blood:
31	chr6:27517580..27520296-chr6:27658437..27660745,2	K562	blood:
32	chr6:27656124..27658141-chr6:27861315..27864462,3	K562	blood:
33	chr6:27660759..27663752-chr6:27861076..27863812,2	K562	blood:
34	chr6:27661232..27663489-chr6:27678201..27680638,2	K562	blood:
35	chr6:27650810..27652452-chr6:27664583..27667295,2	MCF-7	breast:
36	chr6:27596183..27599052-chr6:27654192..27655700,2	K562	blood:
37	chr6:27636299..27636853-chr6:27655225..27655832,2	K562	blood:
38	chr6:27661232..27663489-chr6:27678201..27680638,2	K562	blood:
39	chr6:27651170..27656145-chr6:27660253..27663653,4	MCF-7	breast:
40	chr6:26595641..26598321-chr6:27660238..27661908,2	K562	blood:
41	chr6:27671590..27673866-chr6:27681015..27683164,2	K562	blood:
42	chr6:27568300..27570576-chr6:27654240..27656534,2	K562	blood:
43	chr6:27654225..27656931-chr6:27719778..27721751,2	K562	blood:
44	chr6:27114783..27117247-chr6:27654285..27656648,2	K562	blood:
45	chr6:27653789..27659338-chr6:27659392..27663401,13	K562	blood:
46	chr6:27659790..27663314-chr6:27665578..27668905,6	K562	blood:
47	chr6:27661399..27663799-chr6:27664607..27667603,2	MCF-7	breast:
48	chr6:27676712..27678626-chr6:27679096..27681049,2	K562	blood:
49	chr6:27663855..27666018-chr6:27668315..27670242,2	MCF-7	breast:
50	chr6:27598725..27601418-chr6:27654092..27655925,2	K562	blood:

(count:36 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HIST1H2AI-3	chr6:27670093-27670196	XLOC_005219
2	lnc-HIST1H2AI-3	chr6:27661814-27662285	NONHSAT108395
3	lnc-HIST1H2AI-3	chr6:27674418-27676936	NONHSAT108398
4	lnc-HIST1H2AI-3	chr6:27680783-27681184	NONHSAT108397
5	lnc-HIST1H2AI-2	chr6:27678460-27678668	XLOC_005220
6	lnc-HIST1H2BL-2	chr6:27672903-27672947	NONHSAT108399
7	lnc-HIST1H2AI-3	chr6:27670093-27670196	XLOC_005219
8	lnc-HIST1H2AI-3	chr6:27661843-27662285	NONHSAT108397
9	lnc-HIST1H2AI-3	chr6:27675118-27675276	NONHSAT108397
10	lnc-HIST1H2AI-3	chr6:27670093-27670196	XLOC_005219
11	lnc-HIST1H2AI-3	chr6:27674418-27676935	XLOC_005219
12	lnc-HIST1H2AI-3	chr6:27667376-27667442	NONHSAT108397
13	lnc-HIST1H2AI-3	chr6:27678460-27678670	NONHSAT108397
14	lnc-HIST1H2AI-2	chr6:27677989-27678004	XLOC_005220
15	lnc-HIST1H2AI-3	chr6:27670093-27670196	NONHSAT108395
16	lnc-HIST1H2AI-3	chr6:27675118-27675195	NONHSAT108395
17	lnc-HIST1H2AI-3	chr6:27661814-27662285	XLOC_005219
18	lnc-HIST1H2AI-3	chr6:27661814-27662285	NONHSAT108394
19	lnc-HIST1H2AI-3	chr6:27677903-27678001	NONHSAT108394
20	lnc-HIST1H2AI-3	chr6:27674418-27674530	XLOC_005219
21	lnc-HIST1H2AI-3	chr6:27661814-27662005	XLOC_005219
22	lnc-HIST1H2AI-3	chr6:27670093-27670196	NONHSAT108394
23	lnc-HIST1H2BL-2	chr6:27672956-27673553	NONHSAT108399
24	lnc-HIST1H2AI-3	chr6:27677903-27678001	NONHSAT108395
25	lnc-HIST1H2BL-2	chr6:27680492-27681059	NONHSAT108399
26	lnc-HIST1H2AI-3	chr6:27661814-27662285	XLOC_005219
27	lnc-HIST1H2AI-3	chr6:27670093-27670198	NONHSAT108397
28	lnc-HIST1H2AI-3	chr6:27661858-27662005	ENSG00000246046
29	lnc-HIST1H2AI-3	chr6:27674418-27676935	ENSG00000246046
30	lnc-HIST1H2AI-3	chr6:27661858-27662005	NONHSAT108398
31	lnc-HIST1H2BL-2	chr6:27674985-27675450	NONHSAT108399
32	lnc-HIST1H2AI-3	chr6:27670093-27670196	XLOC_005219
33	lnc-HIST1H2AI-3	chr6:27670093-27670196	ENSG00000246046
34	lnc-HIST1H2AI-2	chr6:27680783-27680876	XLOC_005220
35	lnc-HIST1H2AI-3	chr6:27661865-27662005	XLOC_005219
36	lnc-HIST1H2AI-3	chr6:27670093-27670196	NONHSAT108398

No data

Variant related genes	Relation type
ENSG00000146109	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000203813	chromatin interactions
ENSG00000196331	chromatin interactions
ENSG00000254692	chromatin interactions
ENSG00000196787	chromatin interactions
ENSG00000204444	chromatin interactions
ENSG00000233224	chromatin interactions
ENSG00000198339	chromatin interactions
ENSG00000124635	chromatin interactions
ENSG00000238648	chromatin interactions
ENSG00000254505	chromatin interactions
ENSG00000184825	chromatin interactions
ENSG00000187837	chromatin interactions
ENSG00000204463	chromatin interactions
ENSG00000265565	chromatin interactions
TOP1	miRNA target sites
VAPA	miRNA target sites
BRD8	miRNA target sites
POLR2D	miRNA target sites

Extended variants
information (count: 1113 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1113 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6906653	chr6:27655096-27655097	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563236725	chr6:27655107-27655108	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs528998183	chr6:27655121-27655122	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs548730450	chr6:27655150-27655151	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs374568312	chr6:27655161-27655162	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs115692980	chr6:27655173-27655174	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs528342580	chr6:27655219-27655220	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs551402763	chr6:27655230-27655231	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs552450043	chr6:27655250-27655251	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs368035842	chr6:27655263-27655264	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs116108074	chr6:27655306-27655307	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs142762838	chr6:27655307-27655308	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs556566391	chr6:27655314-27655315	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs186043009	chr6:27655323-27655324	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs76503325	chr6:27655327-27655328	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs570154193	chr6:27655345-27655346	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs535962293	chr6:27655366-27655367	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs555950860	chr6:27655374-27655375	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs572697983	chr6:27655391-27655392	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs570839890	chr6:27655408-27655409	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs190756334	chr6:27655411-27655412	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs73742455	chr6:27655441-27655442	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs578216585	chr6:27655556-27655557	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs1010261	chr6:27655564-27655565	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs563306671	chr6:27655589-27655590	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs568072039	chr6:27655601-27655602	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs62401400	chr6:27655630-27655631	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs535159125	chr6:27655700-27655701	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs528911586	chr6:27655704-27655705	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs181675067	chr6:27655744-27655745	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs559088454	chr6:27655790-27655791	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs371740218	chr6:27655795-27655796	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs528255555	chr6:27655797-27655798	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs372929817	chr6:27655821-27655822	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs565031655	chr6:27655825-27655826	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs186220259	chr6:27655935-27655936	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs549866406	chr6:27655943-27655944	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs570068026	chr6:27655946-27655947	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs191461676	chr6:27655954-27655955	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs182359831	chr6:27655957-27655958	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs188052367	chr6:27655958-27655959	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs190829516	chr6:27655959-27655960	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs183382877	chr6:27655967-27655968	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs578159053	chr6:27655971-27655972	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs375522708	chr6:27655977-27655978	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs9393844	chr6:27655981-27655982	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs556513724	chr6:27655982-27655983	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs573317457	chr6:27655987-27655988	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs1555021	chr6:27655994-27655995	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs376636798	chr6:27655997-27655998	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:901 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:27653600-27656600	Active TSS	HUES6 Cell Line	embryonic stem cell
2	chr6:27654200-27656600	Active TSS	H1 Cell Line	embryonic stem cell
3	chr6:27654600-27656400	Active TSS	HUES48 Cell Line	embryonic stem cell
4	chr6:27654600-27656600	Active TSS	iPS-20b Cell Line	embryonic stem cell
5	chr6:27654800-27655200	Bivalent/Poised TSS	Brain Germinal Matrix	brain
6	chr6:27654800-27655200	Bivalent/Poised TSS	Fetal Brain Female	brain
7	chr6:27654800-27655400	Flanking Active TSS	NHEK	skin
8	chr6:27654800-27656000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr6:27654800-27656200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr6:27654800-27656400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr6:27654800-27656400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr6:27654800-27656400	Active TSS	HMEC	breast
13	chr6:27654800-27656600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr6:27654800-27656600	Active TSS	HUES64 Cell Line	embryonic stem cell
15	chr6:27654800-27656600	Active TSS	iPS-18 Cell Line	embryonic stem cell
16	chr6:27654800-27656600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr6:27654800-27656600	Active TSS	A549	lung
18	chr6:27654800-27656600	Flanking Active TSS	Dnd41	blood
19	chr6:27654800-27657200	Active TSS	K562	blood
20	chr6:27655000-27655200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr6:27655000-27655200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
22	chr6:27655000-27655200	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr6:27655000-27655200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
24	chr6:27655000-27655200	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
25	chr6:27655000-27655200	Active TSS	Primary T cells from cord blood	blood
26	chr6:27655000-27655200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr6:27655000-27655200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
28	chr6:27655000-27655200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
29	chr6:27655000-27655200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
30	chr6:27655000-27655200	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
31	chr6:27655000-27655200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr6:27655000-27655200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr6:27655000-27655200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
34	chr6:27655000-27655200	Bivalent Enhancer	Liver	Liver
35	chr6:27655000-27655200	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
36	chr6:27655000-27655200	Enhancers	Colonic Mucosa	Colon
37	chr6:27655000-27655200	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
38	chr6:27655000-27655200	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
39	chr6:27655000-27655200	Enhancers	Pancreas	Pancrea
40	chr6:27655000-27655200	Active TSS	Rectal Mucosa Donor 29	rectum
41	chr6:27655000-27655200	Active TSS	Right Atrium	heart
42	chr6:27655000-27655200	Enhancers	Spleen	Spleen
43	chr6:27655000-27655200	Flanking Active TSS	GM12878-XiMat	blood
44	chr6:27655000-27655200	Flanking Active TSS	NH-A	brain
45	chr6:27655000-27655200	Flanking Active TSS	Osteobl	bone
46	chr6:27655000-27655400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr6:27655000-27655400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
48	chr6:27655000-27655400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
49	chr6:27655000-27655400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
50	chr6:27655000-27655400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--

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