Variant report

Variant	nsv1036273
Chromosome Location	chr12:34199868-34317832
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:490)
CpG islands
(count:489)
Chromatin interactive
region (count:15)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:34276078-34276334	K562	blood:	n/a	n/a
2	ARID3A	chr12:34276092-34276305	HepG2	liver:	n/a	n/a
3	ATF1	chr12:34280414-34280639	K562	blood:	n/a	n/a
4	ATF1	chr12:34250260-34250470	K562	blood:	n/a	n/a
5	ATF1	chr12:34276078-34276281	K562	blood:	n/a	n/a
6	ATF3	chr12:34280320-34280675	K562	blood:	n/a	n/a
7	ATF3	chr12:34275984-34276254	GM12878	blood:	n/a	n/a
8	BATF	chr12:34207658-34207839	GM12878	blood:	n/a	n/a
9	BATF	chr12:34279173-34279432	GM12878	blood:	n/a	n/a
10	BATF	chr12:34207885-34208102	GM12878	blood:	n/a	n/a
11	BCLAF1	chr12:34275971-34276281	GM12878	blood:	n/a	n/a
12	BCLAF1	chr12:34276036-34276284	GM12878	blood:	n/a	n/a
13	BHLHE40	chr12:34280564-34280568	K562	blood:	n/a	n/a
14	BHLHE40	chr12:34276076-34276276	K562	blood:	n/a	n/a
15	BHLHE40	chr12:34279407-34279583	K562	blood:	n/a	n/a
16	BRCA1	chr12:34295564-34295571	GM12878	blood:	n/a	n/a
17	BRCA1	chr12:34276078-34276312	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr12:34286882-34287265	K562	blood:	n/a	n/a
19	CBX3	chr12:34280367-34280675	K562	blood:	n/a	n/a
20	CBX3	chr12:34280337-34280711	K562	blood:	n/a	n/a
21	CBX3	chr12:34286464-34286764	K562	blood:	n/a	n/a
22	CEBPB	chr12:34276086-34276337	A549	lung:	n/a	n/a
23	CEBPB	chr12:34231038-34231238	HepG2	liver:	n/a	chr12:34231113-34231124
24	CEBPB	chr12:34280269-34280635	K562	blood:	n/a	n/a
25	CEBPB	chr12:34306824-34306969	IMR90	lung:	n/a	n/a
26	CEBPB	chr12:34276029-34276357	IMR90	lung:	n/a	n/a
27	CEBPB	chr12:34276033-34276379	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr12:34276061-34276351	K562	blood:	n/a	n/a
29	CEBPB	chr12:34270808-34271042	K562	blood:	n/a	n/a
30	CEBPB	chr12:34276065-34276346	HepG2	liver:	n/a	n/a
31	CEBPB	chr12:34280240-34280617	K562	blood:	n/a	n/a
32	CEBPB	chr12:34276002-34276280	K562	blood:	n/a	n/a
33	CEBPD	chr12:34280297-34280803	K562	blood:	n/a	n/a
34	CHD2	chr12:34279189-34279391	GM12878	blood:	n/a	n/a
35	CTCF	chr12:34276040-34276190	GM12864	blood:	n/a	n/a
36	CTCF	chr12:34276044-34276367	GM13977	blood:	n/a	n/a
37	CTCF	chr12:34276120-34276270	MCF-7	breast:	n/a	n/a
38	CTCF	chr12:34276200-34276350	HVMF	connective:	n/a	n/a
39	CTCF	chr12:34275960-34276110	GM12870	blood:	n/a	n/a
40	CTCF	chr12:34275974-34276422	IMR90	lung:	n/a	n/a
41	CTCF	chr12:34276019-34276361	MCF-7	breast:	n/a	n/a
42	CTCF	chr12:34284074-34284156	GM13976	blood:	n/a	n/a
43	CTCF	chr12:34276160-34276310	MCF-7	breast:	n/a	n/a
44	CTCF	chr12:34268712-34268761	LNCaP	prostate:	n/a	n/a
45	CTCF	chr12:34276020-34276170	HCM	heart:	n/a	n/a
46	CTCF	chr12:34276120-34276270	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr12:34276040-34276190	GM12874	blood:	n/a	n/a
48	CTCF	chr12:34276040-34276190	BJ	skin:	n/a	n/a
49	CTCF	chr12:34275786-34276345	MCF-7	breast:	n/a	n/a
50	CTCF	chr12:34275883-34276554	K562	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:34317569-34317619	ECC-1	luminal epithelium:	n/a
2	chr12:34317569-34317619	ECC-1	luminal epithelium:	n/a
3	chr12:34259098-34259148	PrEC	prostate:	n/a
4	chr12:34261436-34261486	NHBE	bronchial:	n/a
5	chr12:34261006-34261056	ovcar-3	ovarian:	n/a
6	chr12:34259098-34259148	AoSMC	blood vessel:	n/a
7	chr12:34317569-34317619	GM19239	blood:	n/a
8	chr12:34261436-34261486	Caco-2	colon:	n/a
9	chr12:34260737-34260787	RPTEC	kidney:	n/a
10	chr12:34261436-34261486	GM12892	blood:	n/a
11	chr12:34261436-34261486	GM12878	blood:	n/a
12	chr12:34317569-34317619	HRPEpiC	eye:	n/a
13	chr12:34259098-34259148	PFSK-1	brain:	n/a
14	chr12:34261116-34261166	HL-60	blood:	n/a
15	chr12:34262100-34262150	HCPEpiC	choroid plexus:	n/a
16	chr12:34260737-34260787	NB4	blood:	n/a
17	chr12:34259098-34259148	AG09319	gingival:	n/a
18	chr12:34261006-34261056	AoSMC	blood vessel:	n/a
19	chr12:34262100-34262150	NHBE	bronchial:	n/a
20	chr12:34262100-34262150	GM12878	blood:	n/a
21	chr12:34260737-34260787	AG04449	skin:	fetal
22	chr12:34261436-34261486	U87	brain:	n/a
23	chr12:34260737-34260787	PrEC	prostate:	n/a
24	chr12:34258505-34258555	BE2_C	brain:	n/a
25	chr12:34258505-34258555	HRCEpiC	kidney:	n/a
26	chr12:34259098-34259148	HRE	kidney:	n/a
27	chr12:34259098-34259148	H1-hESC	embryonic stem cell:	embryo
28	chr12:34261436-34261486	MCF10A-Er-Src	breast:	n/a
29	chr12:34261116-34261166	HPAEpiC	pulmonary alveolar:	n/a
30	chr12:34258505-34258555	Hela-S3	cervix:	n/a
31	chr12:34258505-34258555	AG09309	skin:	n/a
32	chr12:34261006-34261056	HRCEpiC	kidney:	n/a
33	chr12:34261116-34261166	NB4	blood:	n/a
34	chr12:34258505-34258555	Caco-2	colon:	n/a
35	chr12:34260737-34260787	HCT-116	colon:	n/a
36	chr12:34259098-34259148	BJ	skin:	n/a
37	chr12:34317569-34317619	HUVEC	blood vessel:	n/a
38	chr12:34317569-34317619	HCPEpiC	choroid plexus:	n/a
39	chr12:34317569-34317619	PANC-1	pancreas:	n/a
40	chr12:34259098-34259148	GM12892	blood:	n/a
41	chr12:34259098-34259148	HL-60	blood:	n/a
42	chr12:34259098-34259148	T-47D	breast:	n/a
43	chr12:34262100-34262150	GM06990	blood:	n/a
44	chr12:34261436-34261486	HRPEpiC	eye:	n/a
45	chr12:34261436-34261486	HEEpiC	esophagus:	n/a
46	chr12:34259098-34259148	ProgFib	skin:	n/a
47	chr12:34261436-34261486	AoSMC	blood vessel:	n/a
48	chr12:34259098-34259148	HRPEpiC	eye:	n/a
49	chr12:34262100-34262150	HMEC	breast:	n/a
50	chr12:34317569-34317619	PFSK-1	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:34275660..34276572-chr12:34778082..34778680,2	MCF-7	breast:
2	chr12:34275135..34276661-chr12:34371105..34372093,8	K562	blood:
3	chr12:34247375..34249864-chr12:34256794..34259523,2	MCF-7	breast:
4	chr12:34276079..34276686-chr12:34371078..34371813,4	MCF-7	breast:
5	chr12:34275785..34276629-chr12:34339119..34339912,4	MCF-7	breast:
6	chr12:34241238..34243550-chr12:38853316..38855678,2	MCF-7	breast:
7	chr12:34275679..34276702-chr12:34339057..34340086,5	MCF-7	breast:
8	chr12:34277684..34280343-chr12:34367543..34370316,2	K562	blood:
9	chr1:227730297..227731134-chr12:34260025..34260625,2	MCF-7	breast:
10	chr12:34247375..34249864-chr12:34256794..34259523,2	MCF-7	breast:
11	chr12:34275803..34276751-chr12:34446099..34446740,3	K562	blood:
12	chr12:34277684..34281105-chr12:34367413..34370316,3	K562	blood:
13	chr12:34275751..34276656-chr12:34370666..34371823,3	MCF-7	breast:
14	chr12:34279057..34280887-chr12:34440053..34441876,2	K562	blood:
15	chr12:34275776..34276287-chr12:34445928..34446780,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALG10-1	chr12:34209496-34209675	ENSG00000256538
2	lnc-ALG10-1	chr12:34208992-34209394	ENSG00000256538
3	lnc-ALG10-1	chr12:34209496-34209704	XLOC_009707
4	lnc-ALG10-2	chr12:34309116-34309255	ENSG00000255628
5	lnc-ALG10-3	chr12:34315397-34315903	NONHSAT027653
6	lnc-ALG10-1	chr12:34208992-34209394	XLOC_009707
7	lnc-ALG10-2	chr12:34315112-34315173	ENSG00000255628
8	lnc-ALG10-2	chr12:34302774-34303105	ENSG00000255628

No data

Variant related genes	Relation type
ENSG00000245482	TF binding region
ENSG00000256986	TF binding region
ENSG00000255628	TF binding region
ENSG00000245482	CpG island
ENSG00000256986	CpG island
ENSG00000255628	CpG island
ENSG00000255652	chromatin interactions
PPARGC1A	miRNA target sites

Extended variants
information (count: 1451 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1451 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530085261	chr12:34201479-34201480	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs370361954	chr12:34201556-34201557	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs192199567	chr12:34201560-34201561	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs571432182	chr12:34201637-34201638	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs368036141	chr12:34201657-34201658	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs118092616	chr12:34201660-34201661	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs553936404	chr12:34201687-34201688	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs184046686	chr12:34201705-34201706	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs375232780	chr12:34201717-34201718	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs545189264	chr12:34201753-34201754	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs114006236	chr12:34201799-34201800	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs187841653	chr12:34201801-34201802	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs189906183	chr12:34201810-34201811	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs565225552	chr12:34201813-34201814	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs112645874	chr12:34201814-34201815	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs541225749	chr12:34201820-34201821	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs561090049	chr12:34201821-34201822	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs182382661	chr12:34201827-34201828	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs550149989	chr12:34201828-34201829	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs187039680	chr12:34201865-34201866	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs531647542	chr12:34201867-34201868	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs113625522	chr12:34201943-34201944	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs551419258	chr12:34201977-34201978	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs149014069	chr12:34201982-34201983	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs528936917	chr12:34201999-34202000	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs111711450	chr12:34202024-34202025	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs74189617	chr12:34202035-34202036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs528458491	chr12:34202076-34202077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs535938528	chr12:34202128-34202129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs35329293	chr12:34202193-34202194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs144945815	chr12:34202267-34202268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs550363355	chr12:34202272-34202273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs10844789	chr12:34202279-34202280	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs538608734	chr12:34202329-34202330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs115349492	chr12:34202364-34202365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572398339	chr12:34202365-34202366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs11053072	chr12:34202399-34202400	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs561096294	chr12:34202400-34202401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs151308829	chr12:34203724-34203725	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs573120175	chr12:34203726-34203727	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs190160788	chr12:34204257-34204258	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs527890496	chr12:34204293-34204294	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs549219972	chr12:34204322-34204323	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs116637019	chr12:34207487-34207488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs567346206	chr12:34207606-34207607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs535878176	chr12:34207612-34207613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs190939515	chr12:34207630-34207631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs115505314	chr12:34207663-34207664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs74073764	chr12:34207693-34207694	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs7358760	chr12:34207763-34207764	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chordoma	18071362	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:200 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:34202000-34202200	Enhancers	A549	lung
2	chr12:34202000-34202400	Enhancers	HepG2	liver
3	chr12:34207400-34207800	Enhancers	Dnd41	blood
4	chr12:34207600-34208000	Enhancers	Primary T helper naive cells from peripheral blood	blood
5	chr12:34207800-34208000	Flanking Active TSS	Dnd41	blood
6	chr12:34207800-34208400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr12:34207800-34208600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
8	chr12:34207800-34209400	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr12:34208000-34208200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
10	chr12:34208000-34208200	Enhancers	Dnd41	blood
11	chr12:34208000-34208400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr12:34208000-34208400	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr12:34208000-34208600	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr12:34208200-34208400	Flanking Active TSS	Dnd41	blood
15	chr12:34208200-34208600	Active TSS	Primary T helper naive cells from peripheral blood	blood
16	chr12:34208400-34209000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr12:34208400-34209000	Enhancers	Dnd41	blood
18	chr12:34250200-34250600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr12:34250400-34251200	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr12:34251200-34251600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr12:34258400-34263200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
22	chr12:34258600-34262800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr12:34259600-34259800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr12:34259800-34260200	Bivalent/Poised TSS	Right Ventricle	heart
25	chr12:34259800-34262800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr12:34260000-34260200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
27	chr12:34260000-34260200	Bivalent Enhancer	Lung	lung
28	chr12:34260000-34261000	Enhancers	Pancreas	Pancrea
29	chr12:34260400-34260800	Bivalent Enhancer	Liver	Liver
30	chr12:34260600-34260800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr12:34260600-34260800	Bivalent Enhancer	Adipose Nuclei	Adipose
32	chr12:34260600-34260800	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
33	chr12:34260600-34262000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr12:34260800-34261000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr12:34260800-34261000	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr12:34260800-34261000	Bivalent Enhancer	Lung	lung
37	chr12:34260800-34261000	Bivalent/Poised TSS	Ovary	ovary
38	chr12:34260800-34261200	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
39	chr12:34260800-34261200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr12:34260800-34261200	Enhancers	Liver	Liver
41	chr12:34260800-34261200	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
42	chr12:34260800-34261400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr12:34260800-34261400	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
44	chr12:34261000-34261200	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr12:34261000-34261200	Flanking Bivalent TSS/Enh	Ovary	ovary
46	chr12:34261000-34261400	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr12:34261000-34261400	Flanking Active TSS	Pancreas	Pancrea
48	chr12:34261000-34261400	Active TSS	Right Atrium	heart
49	chr12:34261200-34261400	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
50	chr12:34261200-34261400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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