Variant report

Variant	nsv541553
Chromosome Location	chr12:84035912-84429867
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1562)
CpG islands
(count:122)
Chromatin interactive
region (count:47)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1562 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:84221618-84221999	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr12:84173481-84173486	K562	blood:	n/a	n/a
3	BATF	chr12:84212767-84212978	GM12878	blood:	n/a	chr12:84212857-84212868
4	BATF	chr12:84339736-84339955	GM12878	blood:	n/a	n/a
5	BATF	chr12:84235450-84235727	GM12878	blood:	n/a	n/a
6	BATF	chr12:84340664-84340866	GM12878	blood:	n/a	n/a
7	BATF	chr12:84340539-84340871	GM12878	blood:	n/a	n/a
8	BCL3	chr12:84199562-84200127	A549	lung:	n/a	n/a
9	BCL3	chr12:84198791-84199422	A549	lung:	n/a	n/a
10	BCL3	chr12:84199451-84200131	A549	lung:	n/a	n/a
11	BCLAF1	chr12:84217463-84217754	GM12878	blood:	n/a	n/a
12	BRCA1	chr12:84206664-84206681	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr12:84238300-84238331	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr12:84217396-84217936	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr12:84217506-84217589	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr12:84273959-84274479	HCT-116	colon:	n/a	n/a
17	CEBPB	chr12:84198853-84199513	A549	lung:	n/a	n/a
18	CEBPB	chr12:84217436-84217770	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr12:84043811-84044018	HepG2	liver:	n/a	chr12:84043854-84043865
20	CEBPB	chr12:84411110-84411439	IMR90	lung:	n/a	chr12:84411290-84411299 chr12:84411288-84411301 chr12:84411289-84411300 chr12:84411288-84411299 chr12:84411290-84411299 chr12:84411290-84411299 chr12:84411288-84411301 chr12:84411288-84411301 chr12:84411290-84411299 chr12:84411288-84411299
21	CEBPB	chr12:84199555-84200085	A549	lung:	n/a	n/a
22	CEBPB	chr12:84375859-84376122	A549	lung:	n/a	n/a
23	CEBPB	chr12:84373516-84373931	A549	lung:	n/a	n/a
24	CEBPB	chr12:84411123-84411392	A549	lung:	n/a	chr12:84411290-84411299 chr12:84411288-84411301 chr12:84411289-84411300 chr12:84411288-84411299 chr12:84411290-84411299 chr12:84411290-84411299 chr12:84411288-84411301 chr12:84411288-84411301 chr12:84411290-84411299 chr12:84411288-84411299
25	CEBPB	chr12:84187455-84187727	A549	lung:	n/a	chr12:84187567-84187578
26	CEBPB	chr12:84187484-84187762	HepG2	liver:	n/a	chr12:84187567-84187578
27	CEBPB	chr12:84362251-84362465	IMR90	lung:	n/a	chr12:84362326-84362337
28	CEBPB	chr12:84287053-84287073	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr12:84422903-84422935	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr12:84138572-84138857	HepG2	liver:	n/a	n/a
31	CEBPB	chr12:84304378-84304634	A549	lung:	n/a	n/a
32	CEBPB	chr12:84212727-84213066	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr12:84286918-84287263	IMR90	lung:	n/a	n/a
34	CEBPB	chr12:84138608-84138887	A549	lung:	n/a	n/a
35	CEBPB	chr12:84187398-84187792	Hela-S3	cervix:	n/a	chr12:84187567-84187578
36	CEBPB	chr12:84352812-84353220	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr12:84138602-84138837	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr12:84280302-84280553	A549	lung:	n/a	n/a
39	CEBPB	chr12:84165274-84165547	HepG2	liver:	n/a	chr12:84165380-84165391
40	CEBPB	chr12:84280298-84280624	IMR90	lung:	n/a	n/a
41	CEBPB	chr12:84212692-84213217	A549	lung:	n/a	n/a
42	CEBPB	chr12:84043724-84044065	Hela-S3	cervix:	n/a	chr12:84043854-84043865
43	CEBPB	chr12:84286987-84287250	A549	lung:	n/a	n/a
44	CEBPB	chr12:84378559-84379340	Hela-S3	cervix:	n/a	chr12:84378661-84378672
45	CEBPB	chr12:84378546-84378780	A549	lung:	n/a	chr12:84378661-84378672
46	CEBPB	chr12:84138536-84138898	IMR90	lung:	n/a	n/a
47	CEBPB	chr12:84365660-84365860	A549	lung:	n/a	n/a
48	CEBPB	chr12:84411124-84411450	HepG2	liver:	n/a	chr12:84411290-84411299 chr12:84411288-84411301 chr12:84411289-84411300 chr12:84411288-84411299 chr12:84411290-84411299 chr12:84411290-84411299 chr12:84411288-84411301 chr12:84411288-84411301 chr12:84411290-84411299 chr12:84411288-84411299
49	CEBPB	chr12:84362208-84362481	HepG2	liver:	n/a	chr12:84362326-84362337
50	CHD1	chr12:84217885-84217889	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:84068532-84068582	HMEC	breast:	n/a
2	chr12:84405423-84405473	HMEC	breast:	n/a
3	chr12:84405423-84405473	SK-N-MC	brain:	n/a
4	chr12:84068532-84068582	AG04450	lung:	fetal
5	chr12:84405423-84405473	HEEpiC	esophagus:	n/a
6	chr12:84405423-84405473	T-47D	breast:	n/a
7	chr12:84405423-84405473	HAEpiC	amniotic membrane:	n/a
8	chr12:84405423-84405473	K562	blood:	n/a
9	chr12:84068532-84068582	HPAEpiC	pulmonary alveolar:	n/a
10	chr12:84068532-84068582	HEEpiC	esophagus:	n/a
11	chr12:84405423-84405473	GM12891	blood:	n/a
12	chr12:84405423-84405473	AG04450	lung:	fetal
13	chr12:84068532-84068582	GM12878	blood:	n/a
14	chr12:84068532-84068582	H1-hESC	embryonic stem cell:	embryo
15	chr12:84068532-84068582	A549	lung:	n/a
16	chr12:84405423-84405473	NHDF-neo	bronchial:	n/a
17	chr12:84068532-84068582	U87	brain:	n/a
18	chr12:84068532-84068582	HCF	heart:	n/a
19	chr12:84405423-84405473	SAEC	small airway:	n/a
20	chr12:84405423-84405473	BE2_C	brain:	n/a
21	chr12:84068532-84068582	MCF-7	breast:	n/a
22	chr12:84405423-84405473	Caco-2	colon:	n/a
23	chr12:84405423-84405473	HCT-116	colon:	n/a
24	chr12:84068532-84068582	AoSMC	blood vessel:	n/a
25	chr12:84405423-84405473	Hepatocyte	liver:	n/a
26	chr12:84405423-84405473	HNPCEpiC	eye:	n/a
27	chr12:84068532-84068582	HNPCEpiC	eye:	n/a
28	chr12:84405423-84405473	PANC-1	pancreas:	n/a
29	chr12:84068532-84068582	HRE	kidney:	n/a
30	chr12:84068532-84068582	Hepatocyte	liver:	n/a
31	chr12:84405423-84405473	AG10803	skin:	n/a
32	chr12:84405423-84405473	SKMC	muscle:	n/a
33	chr12:84068532-84068582	MCF10A-Er-Src	breast:	n/a
34	chr12:84068532-84068582	GM12892	blood:	n/a
35	chr12:84405423-84405473	NT2-D1	testis:	n/a
36	chr12:84405423-84405473	AG09319	gingival:	n/a
37	chr12:84068532-84068582	GM06990	blood:	n/a
38	chr12:84068532-84068582	SAEC	small airway:	n/a
39	chr12:84068532-84068582	HCT-116	colon:	n/a
40	chr12:84405423-84405473	U87	brain:	n/a
41	chr12:84405423-84405473	CMK	blood:	n/a
42	chr12:84068532-84068582	BE2_C	brain:	n/a
43	chr12:84405423-84405473	ovcar-3	ovarian:	n/a
44	chr12:84068532-84068582	SK-N-MC	brain:	n/a
45	chr12:84068532-84068582	BJ	skin:	n/a
46	chr12:84068532-84068582	NT2-D1	testis:	n/a
47	chr12:84405423-84405473	AoSMC	blood vessel:	n/a
48	chr12:84068532-84068582	AG09309	skin:	n/a
49	chr12:84405423-84405473	HEK293	kidney:	embryo
50	chr12:84068532-84068582	GM19239	blood:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:84199392..84199909-chr12:84217037..84217865,2	MCF-7	breast:
2	chr12:83079271..83080216-chr12:84217192..84217878,5	MCF-7	breast:
3	chr12:83077283..83077912-chr12:84217331..84217998,2	MCF-7	breast:
4	chr12:84272692..84275018-chr12:84275623..84277392,2	MCF-7	breast:
5	chr12:84219094..84220507-chr12:84790896..84791617,3	MCF-7	breast:
6	chr12:84138106..84138606-chr20:52739927..52740820,2	MCF-7	breast:
7	chr12:84377626..84380547-chr12:84384455..84387319,2	MCF-7	breast:
8	chr12:84270623..84273533-chr12:84303786..84305748,2	MCF-7	breast:
9	chr12:84190532..84192129-chr12:84200267..84202218,2	K562	blood:
10	chr12:84368464..84370916-chr12:84373444..84375529,2	K562	blood:
11	chr12:84272240..84274157-chr12:84279540..84281050,2	K562	blood:
12	chr12:84219601..84220107-chr12:84891353..84892072,2	MCF-7	breast:
13	chr12:84376018..84379310-chr12:84380855..84384204,3	MCF-7	breast:
14	chr12:84219948..84220960-chr12:84349104..84349647,3	MCF-7	breast:
15	chr12:84372191..84375103-chr12:84384034..84387500,3	K562	blood:
16	chr12:84142380..84143885-chr12:84146991..84148661,2	MCF-7	breast:
17	chr12:84235620..84237833-chr12:84261114..84263120,2	MCF-7	breast:
18	chr12:84276799..84278474-chr20:45988477..45990232,2	MCF-7	breast:
19	chr12:84190532..84192129-chr12:84200267..84202218,2	K562	blood:
20	chr12:84191313..84194252-chr12:84200577..84203127,2	MCF-7	breast:
21	chr12:84298030..84299669-chr12:84301549..84304383,2	K562	blood:
22	chr12:83080291..83081825-chr12:84257884..84260777,2	MCF-7	breast:
23	chr12:84219617..84220155-chr12:84790822..84791366,2	MCF-7	breast:
24	chr12:84142380..84143885-chr12:84146991..84148661,2	MCF-7	breast:
25	chr12:82910494..82911273-chr12:84217531..84218136,2	MCF-7	breast:
26	chr12:84377626..84380547-chr12:84384455..84387319,2	MCF-7	breast:
27	chr12:84031333..84032927-chr12:84034914..84036543,2	MCF-7	breast:
28	chr12:84298030..84299669-chr12:84301549..84304383,2	K562	blood:
29	chr12:84199392..84199909-chr12:84217037..84217865,2	MCF-7	breast:
30	chr1:54192091..54193000-chr12:84272022..84272741,2	MCF-7	breast:
31	chr12:84270623..84273533-chr12:84303786..84305748,2	MCF-7	breast:
32	chr12:84272240..84274157-chr12:84279540..84281050,2	K562	blood:
33	chr12:84372191..84375103-chr12:84384034..84387500,3	K562	blood:
34	chr12:84315911..84318774-chr12:84319552..84322356,2	K562	blood:
35	chr12:84257472..84261320-chr12:84262069..84264682,4	MCF-7	breast:
36	chr12:84315911..84318774-chr12:84319552..84322356,2	K562	blood:
37	chr12:84219646..84220339-chr12:84896793..84897478,2	MCF-7	breast:
38	chr12:84235620..84237833-chr12:84261114..84263120,2	MCF-7	breast:
39	chr12:83079205..83080097-chr12:84217208..84218130,4	MCF-7	breast:
40	chr12:84191313..84194252-chr12:84200577..84203127,2	MCF-7	breast:
41	chr12:83856040..83856789-chr12:84217180..84218034,3	MCF-7	breast:
42	chr12:84368464..84370916-chr12:84373444..84375529,2	K562	blood:
43	chr12:84272692..84275018-chr12:84275623..84277392,2	MCF-7	breast:
44	chr12:84376018..84379310-chr12:84380855..84384204,3	MCF-7	breast:
45	chr12:84219948..84220960-chr12:84349104..84349647,3	MCF-7	breast:
46	chr12:82920722..82921355-chr12:84217213..84217834,2	MCF-7	breast:
47	chr12:84257472..84261320-chr12:84262069..84264682,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC6A15-1	chr12:84054788-84055065	ENSG00000257124.2
2	lnc-SLC6A15-1	chr12:84055208-84055498	ENSG00000257124
3	lnc-SLC6A15-1	chr12:84054863-84055065	ENSG00000257124
4	lnc-SLC6A15-1	chr12:84055208-84055498	ENSG00000257124.2

No data

Variant related genes	Relation type
ENSG00000257124	TF binding region
ENSG00000257124	CpG island
ENSG00000179104	chromatin interactions
HAUS6	miRNA target sites
RBMX	miRNA target sites

Extended variants
information (count: 5355 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:5355 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143343058	chr12:84035967-84035968	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs567188118	chr12:84035976-84035977	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577298006	chr12:84036023-84036024	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546349798	chr12:84036041-84036042	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs146250882	chr12:84036057-84036058	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs6539764	chr12:84036099-84036100	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs536846582	chr12:84036117-84036118	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139392231	chr12:84036127-84036128	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537937682	chr12:84036155-84036156	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555199711	chr12:84036170-84036171	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556033212	chr12:84036171-84036172	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577725799	chr12:84036190-84036191	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376208741	chr12:84036213-84036214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538470798	chr12:84036219-84036220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs7964886	chr12:84036222-84036223	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs367949632	chr12:84036304-84036305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs151177706	chr12:84036342-84036343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149967258	chr12:84036354-84036355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542545130	chr12:84036369-84036370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561735294	chr12:84036393-84036394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573741156	chr12:84036395-84036396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186079446	chr12:84036400-84036401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562853319	chr12:84036433-84036434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs371458017	chr12:84036456-84036457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs145191377	chr12:84036561-84036562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551711942	chr12:84036642-84036643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560698625	chr12:84036694-84036695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs527975171	chr12:84036714-84036715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190883993	chr12:84036745-84036746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372110327	chr12:84036850-84036851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183427858	chr12:84036907-84036908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs76699920	chr12:84036936-84036937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531212436	chr12:84036957-84036958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375150130	chr12:84036997-84036998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116706418	chr12:84037001-84037002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148704715	chr12:84037052-84037053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186903072	chr12:84037069-84037070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553534152	chr12:84037108-84037109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142277190	chr12:84037189-84037190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112623883	chr12:84054817-84054818	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs186946057	chr12:84054934-84054935	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs566800718	chr12:84054976-84054977	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs192474790	chr12:84054990-84054991	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs542839450	chr12:84054991-84054992	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs555932608	chr12:84055005-84055006	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs368876503	chr12:84055024-84055025	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs185030071	chr12:84055025-84055026	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs538413852	chr12:84055030-84055031	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs556496082	chr12:84055041-84055042	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs189879386	chr12:84055059-84055060	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
lymphocytic leukemia	21291569	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:84034800-84037200	Weak transcription	Gastric	stomach
2	chr12:84035800-84036000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:84035800-84036200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr12:84036000-84036200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr12:84054600-84056400	Enhancers	Placenta Amnion	Placenta Amnion
6	chr12:84058400-84058800	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr12:84058400-84058800	Enhancers	Fetal Heart	heart
8	chr12:84058800-84059200	Weak transcription	Fetal Heart	heart
9	chr12:84059200-84060200	Enhancers	Fetal Heart	heart
10	chr12:84059800-84060000	Enhancers	Left Ventricle	heart
11	chr12:84059800-84060200	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr12:84060600-84060800	Enhancers	Left Ventricle	heart
13	chr12:84065400-84068000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr12:84068000-84068800	Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr12:84070400-84072600	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr12:84074000-84074600	Enhancers	Fetal Heart	heart
17	chr12:84074200-84074400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr12:84083800-84084600	Enhancers	NHEK	skin
19	chr12:84084000-84084600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr12:84084000-84084600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr12:84084000-84084600	Enhancers	HMEC	breast
22	chr12:84100400-84103800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:84103800-84105400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:84104200-84105200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
25	chr12:84104600-84105200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
26	chr12:84104600-84105200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr12:84104800-84105200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr12:84105200-84105800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr12:84105200-84106200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr12:84105400-84109000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr12:84111200-84113400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr12:84112600-84113000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr12:84113000-84113200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr12:84113200-84122600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr12:84113400-84113800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
36	chr12:84113400-84113800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
37	chr12:84146600-84147600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr12:84146600-84147600	Enhancers	NHEK	skin
39	chr12:84146800-84147400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr12:84156600-84156800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr12:84156600-84157400	Enhancers	NHEK	skin
42	chr12:84156600-84158000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
43	chr12:84156600-84158400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr12:84156800-84157800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr12:84156800-84158200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr12:84157400-84157800	Flanking Active TSS	NHEK	skin
47	chr12:84157800-84158000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr12:84157800-84158200	Enhancers	NHEK	skin
49	chr12:84158000-84162600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr12:84161600-84163400	Enhancers	Fetal Kidney	kidney

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