Variant report

Variant	nsv877529
Chromosome Location	chr3:136364511-136487559
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2061)
CpG islands
(count:795)
Chromatin interactive
region (count:106)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2061 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:136471085-136472122	HepG2	liver:	n/a	chr3:136471395-136471403
2	ARID3A	chr3:136430438-136430993	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:136469160-136469611	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:136467850-136468195	K562	blood:	n/a	n/a
5	ARID3A	chr3:136408962-136409078	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:136477219-136477570	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:136386046-136386366	K562	blood:	n/a	n/a
8	ARID3A	chr3:136372591-136372893	K562	blood:	n/a	n/a
9	ARID3A	chr3:136391268-136391668	K562	blood:	n/a	n/a
10	ARID3A	chr3:136469214-136470334	K562	blood:	n/a	n/a
11	ARID3A	chr3:136477339-136477618	K562	blood:	n/a	n/a
12	ARID3A	chr3:136471156-136472035	K562	blood:	n/a	chr3:136471395-136471403
13	ARID3A	chr3:136470012-136470555	HepG2	liver:	n/a	n/a
14	ATF1	chr3:136471166-136472105	K562	blood:	n/a	n/a
15	ATF2	chr3:136471110-136472276	GM12878	blood:	n/a	n/a
16	ATF2	chr3:136470998-136471826	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr3:136470948-136471524	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr3:136470994-136472378	GM12878	blood:	n/a	n/a
19	ATF3	chr3:136385891-136386248	K562	blood:	n/a	n/a
20	BACH1	chr3:136471151-136471860	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr3:136400016-136400200	K562	blood:	n/a	n/a
22	BACH1	chr3:136409514-136409718	K562	blood:	n/a	n/a
23	BCL3	chr3:136471643-136472118	A549	lung:	n/a	n/a
24	BCL3	chr3:136471010-136471475	A549	lung:	n/a	chr3:136471407-136471420 chr3:136471333-136471346 chr3:136471383-136471396
25	BCLAF1	chr3:136470998-136472375	GM12878	blood:	n/a	chr3:136471407-136471420 chr3:136471513-136471526 chr3:136471333-136471346 chr3:136471383-136471396 chr3:136471488-136471496
26	BCLAF1	chr3:136469738-136470649	GM12878	blood:	n/a	chr3:136470538-136470547
27	BCLAF1	chr3:136470804-136472384	GM12878	blood:	n/a	chr3:136471407-136471420 chr3:136471513-136471526 chr3:136471333-136471346 chr3:136471383-136471396 chr3:136471488-136471496
28	BHLHE40	chr3:136470944-136472061	HepG2	liver:	n/a	chr3:136471378-136471394 chr3:136471678-136471694
29	BHLHE40	chr3:136470194-136472206	GM12878	blood:	n/a	chr3:136471378-136471394 chr3:136471678-136471694 chr3:136470370-136470386
30	BHLHE40	chr3:136444515-136444621	GM12878	blood:	n/a	n/a
31	BHLHE40	chr3:136470123-136470573	HepG2	liver:	n/a	chr3:136470370-136470386
32	BHLHE40	chr3:136470116-136472342	K562	blood:	n/a	chr3:136471378-136471394 chr3:136471678-136471694 chr3:136470370-136470386
33	BRCA1	chr3:136471161-136471846	GM12878	blood:	n/a	n/a
34	BRCA1	chr3:136471146-136471641	H1-hESC	embryonic stem cell:	n/a	n/a
35	BRCA1	chr3:136390624-136390662	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr3:136471079-136472377	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr3:136470162-136470337	HepG2	liver:	n/a	n/a
38	BRCA1	chr3:136471037-136471914	HepG2	liver:	n/a	n/a
39	CBX3	chr3:136404681-136405157	K562	blood:	n/a	n/a
40	CBX3	chr3:136469910-136470492	K562	blood:	n/a	n/a
41	CBX3	chr3:136471044-136472161	K562	blood:	n/a	n/a
42	CBX3	chr3:136369947-136370224	K562	blood:	n/a	n/a
43	CBX3	chr3:136472720-136473192	K562	blood:	n/a	n/a
44	CBX3	chr3:136411975-136412381	K562	blood:	n/a	n/a
45	CBX3	chr3:136372363-136372889	K562	blood:	n/a	n/a
46	CBX3	chr3:136470026-136470433	K562	blood:	n/a	n/a
47	CBX3	chr3:136372500-136372812	K562	blood:	n/a	n/a
48	CBX3	chr3:136477263-136477653	K562	blood:	n/a	n/a
49	CBX3	chr3:136373463-136373859	HCT-116	colon:	n/a	n/a
50	CBX3	chr3:136481010-136481282	K562	blood:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:136471803-136471853	SK-N-SH_RA	brain:	n/a
2	chr3:136469005-136469055	HCPEpiC	choroid plexus:	n/a
3	chr3:136471803-136471853	SK-N-SH_RA	brain:	n/a
4	chr3:136469005-136469055	HCPEpiC	choroid plexus:	n/a
5	chr3:136471127-136471177	GM06990	blood:	n/a
6	chr3:136471577-136471627	SK-N-MC	brain:	n/a
7	chr3:136471577-136471627	Hela-S3	cervix:	n/a
8	chr3:136471127-136471177	GM12891	blood:	n/a
9	chr3:136377513-136377563	H1-hESC	embryonic stem cell:	embryo
10	chr3:136470434-136470484	AoSMC	blood vessel:	n/a
11	chr3:136471634-136471684	GM19239	blood:	n/a
12	chr3:136469005-136469055	AG04449	skin:	fetal
13	chr3:136471562-136471612	MCF10A-Er-Src	breast:	n/a
14	chr3:136471162-136471212	HRCEpiC	kidney:	n/a
15	chr3:136471577-136471627	AG04450	lung:	fetal
16	chr3:136471577-136471627	AG10803	skin:	n/a
17	chr3:136471127-136471177	HL-60	blood:	n/a
18	chr3:136377513-136377563	AG09309	skin:	n/a
19	chr3:136471634-136471684	HL-60	blood:	n/a
20	chr3:136471127-136471177	AG04450	lung:	fetal
21	chr3:136377513-136377563	SAEC	small airway:	n/a
22	chr3:136377513-136377563	NT2-D1	testis:	n/a
23	chr3:136471376-136471426	AG09319	gingival:	n/a
24	chr3:136471577-136471627	NHBE	bronchial:	n/a
25	chr3:136471162-136471212	ovcar-3	ovarian:	n/a
26	chr3:136471803-136471853	Hela-S3	cervix:	n/a
27	chr3:136471376-136471426	HRPEpiC	eye:	n/a
28	chr3:136471562-136471612	NT2-D1	testis:	n/a
29	chr3:136469005-136469055	AG09309	skin:	n/a
30	chr3:136470434-136470484	AG04449	skin:	fetal
31	chr3:136470434-136470484	U87	brain:	n/a
32	chr3:136377513-136377563	HCPEpiC	choroid plexus:	n/a
33	chr3:136471376-136471426	NT2-D1	testis:	n/a
34	chr3:136469005-136469055	AoSMC	blood vessel:	n/a
35	chr3:136469005-136469055	PANC-1	pancreas:	n/a
36	chr3:136416224-136416274	GM12891	blood:	n/a
37	chr3:136471577-136471627	HUVEC	blood vessel:	n/a
38	chr3:136470434-136470484	PrEC	prostate:	n/a
39	chr3:136471577-136471627	NHDF-neo	bronchial:	n/a
40	chr3:136471803-136471853	K562	blood:	n/a
41	chr3:136416224-136416274	Jurkat	blood:	n/a
42	chr3:136468191-136468241	NHDF-neo	bronchial:	n/a
43	chr3:136470434-136470484	MCF-7	breast:	n/a
44	chr3:136468191-136468241	HRPEpiC	eye:	n/a
45	chr3:136470434-136470484	HUVEC	blood vessel:	n/a
46	chr3:136471634-136471684	HPAEpiC	pulmonary alveolar:	n/a
47	chr3:136468191-136468241	T-47D	breast:	n/a
48	chr3:136471376-136471426	HMEC	breast:	n/a
49	chr3:136469005-136469055	GM12891	blood:	n/a
50	chr3:136471162-136471212	AG09319	gingival:	n/a

(count:106 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr3:136366127..136367827-chr3:136383868..136385669,2	K562	blood:
2	chr3:136471103..136473077-chr3:136487227..136489991,3	MCF-7	breast:
3	chr3:136405715..136407497-chr3:136411173..136412850,2	K562	blood:
4	chr3:136371791..136373767-chr3:136377876..136379959,2	MCF-7	breast:
5	chr3:136460640..136463485-chr3:136464653..136466977,3	K562	blood:
6	chr3:136049332..136050837-chr3:136449297..136451050,2	MCF-7	breast:
7	chr3:136472151..136474742-chr3:136749777..136751390,2	K562	blood:
8	chr3:136309415..136311669-chr3:136473283..136476207,2	K562	blood:
9	chr3:136447967..136449476-chr3:136469163..136470945,2	MCF-7	breast:
10	chr3:135968756..135970580-chr3:136469634..136471998,2	K562	blood:
11	chr3:136208388..136211090-chr3:136467197..136470066,2	K562	blood:
12	chr3:136477513..136478380-chr3:136668652..136669180,2	MCF-7	breast:
13	chr11:62609047..62610004-chr3:136469655..136471390,4	Hela-S3	cervix:
14	chr3:135967505..135970256-chr3:136469769..136472442,3	K562	blood:
15	chr3:136447967..136449476-chr3:136469163..136470945,2	MCF-7	breast:
16	chr3:136389835..136392302-chr3:136408179..136409824,2	MCF-7	breast:
17	chr3:136422396..136423901-chr3:136425473..136427941,2	MCF-7	breast:
18	chr3:136457290..136459900-chr3:136462438..136464263,2	K562	blood:
19	chr3:136477054..136477907-chr3:136732416..136733197,2	K562	blood:
20	chr3:136469311..136474326-chr3:136579207..136583133,7	K562	blood:
21	chr3:136469358..136473351-chr3:136579831..136582888,9	MCF-7	breast:
22	chr3:133969194..133969719-chr3:136470769..136471350,2	Hela-S3	cervix:
23	chr3:136362757..136364544-chr3:136367826..136369357,2	MCF-7	breast:
24	chr3:136476053..136479031-chr3:136579803..136582728,2	K562	blood:
25	chr3:136457793..136459867-chr3:136469350..136471388,2	MCF-7	breast:
26	chr3:136366127..136367827-chr3:136383868..136385669,2	K562	blood:
27	chr3:136371597..136373384-chr3:136469509..136471218,2	K562	blood:
28	chr3:136389263..136391478-chr3:136467252..136469430,2	K562	blood:
29	chr1:153747489..153748173-chr3:136470178..136470949,2	Hela-S3	cervix:
30	chr3:136399125..136401891-chr3:136427700..136429759,2	MCF-7	breast:
31	chr3:135968107..135969967-chr3:136470513..136472370,2	MCF-7	breast:
32	chr3:136477479..136478033-chr3:136732451..136733138,2	MCF-7	breast:
33	chr12:7053185..7053691-chr3:136471368..136471965,2	Hela-S3	cervix:
34	chr3:136261604..136263396-chr3:136467886..136469461,2	K562	blood:
35	chr3:136471576..136472305-chr3:136732784..136733377,2	MCF-7	breast:
36	chr3:136447920..136449484-chr3:136469466..136471753,2	K562	blood:
37	chr3:136470105..136470853-chr3:195269618..195270475,2	Hela-S3	cervix:
38	chr3:136380655..136383814-chr3:136385853..136389244,3	MCF-7	breast:
39	chr3:136471501..136472073-chr7:6143796..6144617,2	Hela-S3	cervix:
40	chr19:12901783..12902716-chr3:136470756..136471316,2	Hela-S3	cervix:
41	chr3:136377566..136379306-chr3:136381547..136383907,2	K562	blood:
42	chr3:136472622..136474527-chr3:136477300..136478827,2	K562	blood:
43	chr3:136388635..136392149-chr3:136467930..136472508,4	K562	blood:
44	chr3:136405715..136407497-chr3:136411173..136412850,2	K562	blood:
45	chr3:136429151..136431156-chr3:137893045..137894815,2	MCF-7	breast:
46	chr3:136460807..136463236-chr3:136469569..136471141,2	MCF-7	breast:
47	chr1:28832529..28833084-chr3:136470773..136471712,2	HCT-116	colon:
48	chr3:135912902..135916874-chr3:136469598..136473232,8	MCF-7	breast:
49	chr3:136470133..136470947-chrX:41193764..41194501,2	Hela-S3	cervix:
50	chr3:136364480..136366014-chr3:136376930..136379520,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MSL2-6	chr3:136455342-136456071	NONHSAT092281
2	lnc-TMEM22-1	chr3:136472487-136472720	NONHSAT092283
3	lnc-STAG1-4	chr3:136486167-136486437	NONHSAT092284
4	lnc-TMEM22-1	chr3:136471472-136474622	ENSG00000261758.1

No data

Variant related genes	Relation type
RNU6-789P	TF binding region
ENSG00000261758	TF binding region
ENSG00000240695	TF binding region
STAG1	TF binding region
RNU6-789P	CpG island
ENSG00000261758	CpG island
ENSG00000240695	CpG island
STAG1	CpG island
ENSG00000106346	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000114054	chromatin interactions
ENSG00000184203	chromatin interactions
ENSG00000251708	chromatin interactions
ENSG00000202408	chromatin interactions
ENSG00000174579	chromatin interactions
ENSG00000118007	chromatin interactions
ENSG00000196542	chromatin interactions
ENSG00000171223	chromatin interactions
ENSG00000239213	chromatin interactions
ENSG00000168917	chromatin interactions
ENSG00000240695	chromatin interactions
ENSG00000185305	chromatin interactions
ENSG00000242125	chromatin interactions
ENSG00000215301	chromatin interactions
ENSG00000143554	chromatin interactions
ENSG00000158169	chromatin interactions
ENSG00000138231	chromatin interactions
ENSG00000261758	chromatin interactions
ENSG00000122642	chromatin interactions
ENSG00000180198	chromatin interactions
ENSG00000163874	chromatin interactions
ENSG00000158092	chromatin interactions
ENSG00000118412	chromatin interactions
ENSG00000115539	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000163785	chromatin interactions
ENSG00000144802	chromatin interactions

Extended variants
information (count: 4394 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:4394 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7646723	chr3:136364511-136364512	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs541655530	chr3:136364535-136364536	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs532367600	chr3:136364539-136364540	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs561923012	chr3:136364567-136364568	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs552164874	chr3:136364576-136364577	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs575405544	chr3:136364637-136364638	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs112063043	chr3:136364641-136364642	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs563313427	chr3:136364665-136364666	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs115059544	chr3:136364725-136364726	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs191754727	chr3:136364739-136364740	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs559414413	chr3:136364749-136364750	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs183602606	chr3:136364767-136364768	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs548450020	chr3:136364776-136364777	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs28390205	chr3:136364850-136364851	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs551318507	chr3:136364855-136364856	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs145068006	chr3:136364856-136364857	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs571191634	chr3:136364912-136364913	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs539429132	chr3:136364919-136364920	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs185812480	chr3:136364933-136364934	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs190332256	chr3:136365036-136365037	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs138811245	chr3:136365050-136365051	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs116463502	chr3:136365062-136365063	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs555233739	chr3:136365066-136365067	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs59931907	chr3:136365097-136365098	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs544028734	chr3:136365113-136365114	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs557616590	chr3:136365137-136365138	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs182561541	chr3:136365180-136365181	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs559716178	chr3:136365215-136365216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545792809	chr3:136365348-136365349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs559702585	chr3:136365357-136365358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs554102250	chr3:136365371-136365372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs186832037	chr3:136365396-136365397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542324963	chr3:136365447-136365448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs6767889	chr3:136365455-136365456	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs34164990	chr3:136365457-136365458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546436870	chr3:136365462-136365463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs531105953	chr3:136365488-136365489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551234779	chr3:136365516-136365517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571157780	chr3:136365531-136365532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533670345	chr3:136365555-136365556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192537392	chr3:136365567-136365568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547724632	chr3:136365620-136365621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs535171250	chr3:136365678-136365679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs555416251	chr3:136365701-136365702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs1298459	chr3:136365702-136365703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs537642068	chr3:136365748-136365749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs557579769	chr3:136365750-136365751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577471618	chr3:136365764-136365765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs540149698	chr3:136365813-136365814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs553058287	chr3:136365818-136365819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18511947	CNVD
Breast cancer	22522925	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:2893 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:136336200-136364800	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr3:136347200-136368400	Weak transcription	Fetal Intestine Small	intestine
3	chr3:136347600-136367200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr3:136348200-136365000	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr3:136348600-136364600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr3:136348800-136373600	Weak transcription	Thymus	Thymus
7	chr3:136349800-136372400	Weak transcription	Dnd41	blood
8	chr3:136350600-136372200	Weak transcription	Primary T cells from cord blood	blood
9	chr3:136351600-136364600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr3:136351600-136364800	Weak transcription	Pancreas	Pancrea
11	chr3:136351600-136376200	Weak transcription	Esophagus	oesophagus
12	chr3:136351800-136364600	Weak transcription	Right Ventricle	heart
13	chr3:136352400-136371600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr3:136352400-136371600	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr3:136352400-136371800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr3:136356000-136364600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr3:136357800-136368200	Weak transcription	Lung	lung
18	chr3:136357800-136387400	Weak transcription	Fetal Thymus	thymus
19	chr3:136361400-136366200	Weak transcription	Fetal Stomach	stomach
20	chr3:136361800-136364600	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr3:136362000-136364800	Weak transcription	K562	blood
22	chr3:136363600-136365000	Enhancers	Ovary	ovary
23	chr3:136363600-136365200	Enhancers	Psoas Muscle	Psoas
24	chr3:136363600-136365400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr3:136364000-136364600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr3:136364000-136365000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr3:136364000-136365000	Enhancers	Small Intestine	intestine
28	chr3:136364000-136366200	Enhancers	Primary T helper cells PMA-I stimulated	--
29	chr3:136364200-136364600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr3:136364200-136365200	Flanking Active TSS	GM12878-XiMat	blood
31	chr3:136364200-136368000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr3:136364400-136364800	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr3:136364400-136369400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr3:136364600-136364800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr3:136364600-136364800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr3:136364600-136364800	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr3:136364600-136365000	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr3:136364600-136365000	Enhancers	Gastric	stomach
39	chr3:136364600-136365200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr3:136364600-136365200	Enhancers	Right Ventricle	heart
41	chr3:136364600-136371800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr3:136364800-136365000	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr3:136364800-136365200	Enhancers	Primary B cells from peripheral blood	blood
44	chr3:136364800-136365200	Enhancers	Pancreas	Pancrea
45	chr3:136364800-136365200	Enhancers	K562	blood
46	chr3:136364800-136368000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr3:136364800-136372200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr3:136364800-136377800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr3:136365000-136365200	Enhancers	Primary T cells fromperipheralblood	blood
50	chr3:136365000-136370000	Weak transcription	Ovary	ovary

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