Variant report

Variant	nsv1025413
Chromosome Location	chr6:57208043-57617947
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4141)
CpG islands
(count:1037)
Chromatin interactive
region (count:88)
LncRNA
region (count:7)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:4141 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:57445284-57445884	K562	blood:	n/a	n/a
2	ARID3A	chr6:57236576-57237274	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:57392130-57392164	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:57364923-57365929	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:57445471-57445872	HepG2	liver:	n/a	n/a
6	ATF1	chr6:57296724-57296768	K562	blood:	n/a	n/a
7	ATF1	chr6:57433964-57434331	K562	blood:	n/a	n/a
8	ATF1	chr6:57483250-57483369	K562	blood:	n/a	n/a
9	ATF1	chr6:57487670-57487865	K562	blood:	n/a	n/a
10	ATF1	chr6:57388328-57388901	K562	blood:	n/a	n/a
11	ATF1	chr6:57414346-57414465	K562	blood:	n/a	n/a
12	ATF1	chr6:57483779-57483974	K562	blood:	n/a	n/a
13	ATF1	chr6:57422764-57422956	K562	blood:	n/a	n/a
14	ATF1	chr6:57386257-57386379	K562	blood:	n/a	n/a
15	ATF1	chr6:57529957-57530116	K562	blood:	n/a	n/a
16	ATF1	chr6:57573821-57574021	K562	blood:	n/a	n/a
17	ATF1	chr6:57329848-57330048	K562	blood:	n/a	n/a
18	ATF1	chr6:57432706-57432903	K562	blood:	n/a	n/a
19	ATF2	chr6:57288321-57288802	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr6:57288167-57288786	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr6:57365814-57365865	K562	blood:	n/a	n/a
22	BACH1	chr6:57337567-57337643	K562	blood:	n/a	n/a
23	BACH1	chr6:57501831-57501836	K562	blood:	n/a	n/a
24	BACH1	chr6:57408878-57409078	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr6:57486231-57486242	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr6:57419536-57419915	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr6:57334050-57334159	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr6:57545381-57545540	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr6:57526352-57526945	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr6:57288493-57288790	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr6:57388299-57388865	K562	blood:	n/a	n/a
32	BACH1	chr6:57350106-57350125	K562	blood:	n/a	n/a
33	BACH1	chr6:57541125-57541357	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr6:57363671-57363854	K562	blood:	n/a	n/a
35	BACH1	chr6:57439570-57440015	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr6:57364094-57364109	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr6:57305657-57305828	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr6:57269047-57269216	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr6:57488136-57488168	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr6:57228847-57228853	K562	blood:	n/a	n/a
41	BATF	chr6:57254076-57254287	GM12878	blood:	n/a	chr6:57254189-57254200
42	BATF	chr6:57215182-57215534	GM12878	blood:	n/a	n/a
43	BATF	chr6:57213914-57214212	GM12878	blood:	n/a	n/a
44	BCL11A	chr6:57284786-57285093	GM12878	blood:	n/a	n/a
45	BCL11A	chr6:57288290-57288688	H1-hESC	embryonic stem cell:	n/a	n/a
46	BCL11A	chr6:57284708-57285068	GM12878	blood:	n/a	n/a
47	BCL11A	chr6:57288294-57288755	H1-hESC	embryonic stem cell:	n/a	n/a
48	BHLHE40	chr6:57396741-57396999	GM12878	blood:	n/a	n/a
49	BHLHE40	chr6:57450923-57451339	A549	lung:	n/a	n/a
50	BHLHE40	chr6:57519324-57519409	K562	blood:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:57306409-57306459	GM19239	blood:	n/a
2	chr6:57305889-57305939	CMK	blood:	n/a
3	chr6:57339858-57339908	A549	lung:	n/a
4	chr6:57245939-57245989	AG04449	skin:	fetal
5	chr6:57359134-57359184	BJ	skin:	n/a
6	chr6:57339858-57339908	BJ	skin:	n/a
7	chr6:57339858-57339908	Hela-S3	cervix:	n/a
8	chr6:57218853-57218903	NH-A	brain:	n/a
9	chr6:57305889-57305939	Hela-S3	cervix:	n/a
10	chr6:57253598-57253648	GM12892	blood:	n/a
11	chr6:57306409-57306459	GM06990	blood:	n/a
12	chr6:57385844-57385894	NHBE	bronchial:	n/a
13	chr6:57384347-57384397	AG10803	skin:	n/a
14	chr6:57335405-57335455	HRE	kidney:	n/a
15	chr6:57253598-57253648	AoSMC	blood vessel:	n/a
16	chr6:57391815-57391865	RPTEC	kidney:	n/a
17	chr6:57350270-57350320	AG09309	skin:	n/a
18	chr6:57288411-57288461	AG09319	gingival:	n/a
19	chr6:57218853-57218903	HUVEC	blood vessel:	n/a
20	chr6:57391815-57391865	LNCaP	prostate:	n/a
21	chr6:57385844-57385894	ECC-1	luminal epithelium:	n/a
22	chr6:57339858-57339908	HEEpiC	esophagus:	n/a
23	chr6:57335405-57335455	Hela-S3	cervix:	n/a
24	chr6:57385844-57385894	MCF-7	breast:	n/a
25	chr6:57350270-57350320	AG04449	skin:	fetal
26	chr6:57391815-57391865	PFSK-1	brain:	n/a
27	chr6:57245939-57245989	PrEC	prostate:	n/a
28	chr6:57384347-57384397	HRCEpiC	kidney:	n/a
29	chr6:57350270-57350320	HRCEpiC	kidney:	n/a
30	chr6:57391815-57391865	CMK	blood:	n/a
31	chr6:57272398-57272448	HPAEpiC	pulmonary alveolar:	n/a
32	chr6:57339858-57339908	Hepatocyte	liver:	n/a
33	chr6:57447898-57447948	PFSK-1	brain:	n/a
34	chr6:57253598-57253648	BE2_C	brain:	n/a
35	chr6:57384347-57384397	HPAEpiC	pulmonary alveolar:	n/a
36	chr6:57335405-57335455	NHDF-neo	bronchial:	n/a
37	chr6:57235407-57235457	Hepatocyte	liver:	n/a
38	chr6:57350270-57350320	SAEC	small airway:	n/a
39	chr6:57335405-57335455	GM12892	blood:	n/a
40	chr6:57614321-57614371	AoSMC	blood vessel:	n/a
41	chr6:57306409-57306459	SK-N-MC	brain:	n/a
42	chr6:57288411-57288461	GM12892	blood:	n/a
43	chr6:57235407-57235457	AG10803	skin:	n/a
44	chr6:57288411-57288461	HCF	heart:	n/a
45	chr6:57253598-57253648	HCM	heart:	n/a
46	chr6:57253598-57253648	Hela-S3	cervix:	n/a
47	chr6:57350270-57350320	HNPCEpiC	eye:	n/a
48	chr6:57335405-57335455	NH-A	brain:	n/a
49	chr6:57272398-57272448	HMEC	breast:	n/a
50	chr6:57235407-57235457	BE2_C	brain:	n/a

(count:88 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:57371365..57373576-chr6:57373848..57375922,2	K562	blood:
2	chr6:57226391..57228337-chr6:57232279..57234513,2	K562	blood:
3	chr6:57214841..57217586-chr6:57224303..57226247,2	K562	blood:
4	chr6:57368098..57370585-chr6:57379961..57384432,3	K562	blood:
5	chr6:57232895..57235001-chr6:57373838..57375777,2	K562	blood:
6	chr3:81978758..81979420-chr6:57518103..57518962,2	MCF-7	breast:
7	chr6:57460058..57461813-chr6:57464595..57467531,2	MCF-7	breast:
8	chr6:57437551..57439992-chr6:57443844..57446833,2	K562	blood:
9	chr6:57209967..57212539-chr6:57213014..57215856,3	MCF-7	breast:
10	chr6:57370604..57372865-chr6:57373848..57376238,2	K562	blood:
11	chr5:21570110..21571992-chr6:57575867..57577390,2	K562	blood:
12	chr6:57349293..57351634-chr6:57356907..57359151,3	MCF-7	breast:
13	chr6:57229138..57231697-chr6:57233407..57236328,3	K562	blood:
14	chr6:57371365..57373576-chr6:57373848..57375922,2	K562	blood:
15	chr6:57445367..57446031-chr6:62860058..62860574,2	MCF-7	breast:
16	chr6:57445250..57446013-chr6:57537509..57538705,3	MCF-7	breast:
17	chr6:57413449..57416181-chr6:57416496..57418603,2	K562	blood:
18	chr6:57380965..57383908-chr6:57390419..57392004,2	K562	blood:
19	chr6:57296504..57298287-chr6:57300033..57301535,2	K562	blood:
20	chr6:57541185..57543919-chr8:104728155..104729992,2	MCF-7	breast:
21	chr6:57244329..57246093-chr6:57248866..57250667,2	K562	blood:
22	chr6:57214841..57217586-chr6:57224303..57226247,2	K562	blood:
23	chr6:57405693..57407850-chr6:57408076..57409919,2	K562	blood:
24	chr6:57302195..57303819-chr6:57305158..57307849,2	MCF-7	breast:
25	chr6:57444969..57446432-chr6:57539130..57540030,7	MCF-7	breast:
26	chr6:57287892..57290689-chr6:57302857..57304913,2	K562	blood:
27	chr6:57229138..57231697-chr6:57233407..57236328,3	K562	blood:
28	chr6:57489928..57492575-chr6:57494690..57497411,2	K562	blood:
29	chr6:57370604..57372865-chr6:57373848..57376238,2	K562	blood:
30	chr6:57297598..57300578-chr6:57301764..57305557,4	K562	blood:
31	chr6:57346719..57348670-chr6:57349128..57351994,2	MCF-7	breast:
32	chr6:57232895..57235001-chr6:57373838..57375777,2	K562	blood:
33	chr6:57358740..57361214-chr6:57362213..57364300,2	K562	blood:
34	chr11:17753668..17754453-chr6:57615850..57616702,2	MCF-7	breast:
35	chr6:57380965..57383908-chr6:57390419..57392004,2	K562	blood:
36	chr6:57217129..57218039-chr6:57539079..57539990,3	MCF-7	breast:
37	chr6:57405693..57407850-chr6:57408076..57409919,2	K562	blood:
38	chr6:57396857..57397774-chr9:95368803..95369303,2	MCF-7	breast:
39	chr6:57344628..57347602-chr6:57348060..57349813,2	K562	blood:
40	chr6:57302195..57303819-chr6:57305158..57307849,2	MCF-7	breast:
41	chr6:57217129..57218039-chr6:57539079..57539990,3	MCF-7	breast:
42	chr6:57489928..57492575-chr6:57494690..57497411,2	K562	blood:
43	chr6:57421846..57424167-chr6:57427801..57430462,3	MCF-7	breast:
44	chr6:57394320..57396660-chr6:58286293..58287831,2	MCF-7	breast:
45	chr6:57445356..57445958-chr6:57689666..57690275,2	MCF-7	breast:
46	chr6:57297690..57300107-chr6:57303137..57305465,2	MCF-7	breast:
47	chr6:57429189..57431102-chr6:57440501..57442862,2	MCF-7	breast:
48	chr6:57293162..57295571-chr6:57300739..57302981,3	K562	blood:
49	chr6:57344628..57347602-chr6:57348060..57349813,2	K562	blood:
50	chr6:57198328..57200503-chr6:57228180..57229836,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAB23-12	chr6:57543887-57544127	NONHSAT113297
2	lnc-RAB23-9	chr6:57236060-57236103	ucscGeneNc_uc003pdu_1
3	lnc-RAB23-9	chr6:57233281-57234474	ucscGeneNc_uc003pdu_1
4	lnc-RAB23-12	chr6:57551484-57551584	NONHSAT113297
5	lnc-BAG2-1	chr6:57362331-57362565	ENSG00000266579.1
6	lnc-BAG2-1	chr6:57358736-57358845	ENSG00000266579.1
7	lnc-RAB23-9	chr6:57235203-57235424	ucscGeneNc_uc003pdu_1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548u	chr6:57254978-57255000	MIMAT0015013

No data

Variant related genes	Relation type
MIR548U	TF binding region
PRIM2	TF binding region
ENSG00000266579	TF binding region
MIR548U	CpG island
PRIM2	CpG island
ENSG00000266579	CpG island
ENSG00000146143	chromatin interactions
ENSG00000266579	chromatin interactions
ENSG00000215190	chromatin interactions
ENSG00000263745	chromatin interactions

Extended variants
information (count: 23051 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:23051 , 50 per page) page: 1 2 3 4 5 6 7 ... 462

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531719867	chr6:57208110-57208111	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs744659	chr6:57208153-57208154	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550100991	chr6:57208159-57208160	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs12662732	chr6:57208168-57208169	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555145855	chr6:57208183-57208184	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs60682850	chr6:57208212-57208213	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532577735	chr6:57208251-57208252	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201701915	chr6:57208284-57208285	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs66486048	chr6:57208285-57208286	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs13218946	chr6:57208306-57208307	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs9464441	chr6:57208351-57208352	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs78381429	chr6:57208365-57208366	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547665330	chr6:57208366-57208367	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566057545	chr6:57208368-57208369	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536415524	chr6:57208370-57208371	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs77599312	chr6:57208371-57208372	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554754232	chr6:57208378-57208379	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs13218978	chr6:57208387-57208388	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs3800015	chr6:57208396-57208397	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs537542814	chr6:57208440-57208441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs556265704	chr6:57208470-57208471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577551877	chr6:57208472-57208473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs9464442	chr6:57208503-57208504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs9382702	chr6:57208509-57208510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs9382703	chr6:57208523-57208524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs374564663	chr6:57208555-57208556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs545049972	chr6:57208569-57208570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs554080746	chr6:57208582-57208583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572385234	chr6:57208601-57208602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs542802543	chr6:57208612-57208613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561064983	chr6:57208618-57208619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs111762135	chr6:57208630-57208631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs374641241	chr6:57208638-57208639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs9396275	chr6:57208648-57208649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs116727640	chr6:57208651-57208652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs543539464	chr6:57208693-57208694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs9382704	chr6:57208705-57208706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs190095029	chr6:57208721-57208722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs9475857	chr6:57208727-57208728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs532376323	chr6:57208765-57208766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs9382705	chr6:57208793-57208794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547405741	chr6:57208799-57208800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs9367720	chr6:57208805-57208806	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528601502	chr6:57208821-57208822	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565993946	chr6:57208827-57208828	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs530333052	chr6:57208828-57208829	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs548518263	chr6:57208882-57208883	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs570141387	chr6:57208919-57208920	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs113683654	chr6:57208923-57208924	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs555963729	chr6:57208940-57208941	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	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
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	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
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	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
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:3203 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:57194600-57214800	Weak transcription	Small Intestine	intestine
2	chr6:57194600-57215200	Weak transcription	Ovary	ovary
3	chr6:57194600-57226200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr6:57194600-57244800	Weak transcription	Spleen	Spleen
5	chr6:57194800-57211600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr6:57195600-57212600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr6:57195600-57238400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr6:57198200-57212400	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr6:57199000-57213800	Weak transcription	K562	blood
10	chr6:57199600-57211800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr6:57199600-57213200	Weak transcription	HSMM	muscle
12	chr6:57199600-57213400	Weak transcription	Fetal Thymus	thymus
13	chr6:57199600-57214600	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr6:57199600-57214800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr6:57199600-57215200	Weak transcription	Osteobl	bone
16	chr6:57199600-57221000	Weak transcription	Hela-S3	cervix
17	chr6:57199600-57229000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:57199800-57208200	Weak transcription	Rectal Smooth Muscle	rectum
19	chr6:57199800-57210600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr6:57199800-57210600	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr6:57199800-57210800	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr6:57199800-57210800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr6:57199800-57210800	Weak transcription	Primary B cells from cord blood	blood
24	chr6:57199800-57210800	Weak transcription	Dnd41	blood
25	chr6:57199800-57211600	Weak transcription	NHLF	lung
26	chr6:57199800-57213200	Weak transcription	Primary B cells from peripheral blood	blood
27	chr6:57199800-57213400	Weak transcription	Primary hematopoietic stem cells	blood
28	chr6:57199800-57213800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr6:57199800-57214600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr6:57199800-57251000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr6:57200000-57218000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr6:57200600-57215000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr6:57206200-57208600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr6:57206400-57209200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr6:57206400-57211600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr6:57206800-57208200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr6:57206800-57210000	Weak transcription	Thymus	Thymus
38	chr6:57206800-57210400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr6:57207000-57210400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr6:57207600-57208200	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr6:57207600-57208400	Strong transcription	NHDF-Ad	bronchial
42	chr6:57207600-57208800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr6:57207800-57210000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr6:57208200-57208400	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr6:57208200-57208800	Enhancers	Psoas Muscle	Psoas
46	chr6:57208400-57211400	Weak transcription	NHDF-Ad	bronchial
47	chr6:57208600-57208800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr6:57208600-57210200	Enhancers	GM12878-XiMat	blood
49	chr6:57208800-57209000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr6:57208800-57210800	Weak transcription	H1 Cell Line	embryonic stem cell

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