Variant report

Variant	nsv602
Chromosome Location	chr12:9609303-9748494
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:610)
CpG islands
(count:306)
Chromatin interactive
region (count:5)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:9621679-9621874	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:9740655-9741170	K562	blood:	n/a	n/a
3	ARID3A	chr12:9743025-9743373	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:9741257-9741854	HepG2	liver:	n/a	n/a
5	ATF1	chr12:9740572-9740926	K562	blood:	n/a	n/a
6	BACH1	chr12:9740595-9741065	K562	blood:	n/a	n/a
7	BACH1	chr12:9740652-9740897	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr12:9623145-9623344	GM12878	blood:	n/a	n/a
9	BATF	chr12:9627071-9627414	GM12878	blood:	n/a	chr12:9627229-9627240
10	BATF	chr12:9627069-9627370	GM12878	blood:	n/a	chr12:9627229-9627240
11	BHLHE40	chr12:9621680-9621866	K562	blood:	n/a	n/a
12	BRCA1	chr12:9621725-9621746	GM12878	blood:	n/a	n/a
13	CCNT2	chr12:9740427-9741071	K562	blood:	n/a	n/a
14	CEBPB	chr12:9621719-9621810	K562	blood:	n/a	n/a
15	CEBPB	chr12:9635038-9635326	IMR90	lung:	n/a	chr12:9635144-9635153 chr12:9635144-9635153 chr12:9635144-9635153
16	CEBPB	chr12:9699973-9700136	IMR90	lung:	n/a	n/a
17	CEBPB	chr12:9621557-9621862	HepG2	liver:	n/a	n/a
18	CEBPB	chr12:9626941-9627031	K562	blood:	n/a	chr12:9626967-9626978
19	CEBPB	chr12:9621651-9621793	HepG2	liver:	n/a	n/a
20	CEBPB	chr12:9728216-9728457	A549	lung:	n/a	n/a
21	CEBPB	chr12:9699995-9700109	A549	lung:	n/a	n/a
22	CEBPB	chr12:9626864-9627128	K562	blood:	n/a	chr12:9626967-9626978
23	CEBPB	chr12:9626823-9627139	HepG2	liver:	n/a	chr12:9626967-9626978
24	CEBPB	chr12:9741394-9741705	HepG2	liver:	n/a	n/a
25	CEBPB	chr12:9646117-9646284	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr12:9626847-9627088	A549	lung:	n/a	chr12:9626967-9626978
27	CEBPB	chr12:9621705-9621858	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr12:9626831-9627127	Hela-S3	cervix:	n/a	chr12:9626967-9626978
29	CEBPZ	chr12:9741497-9741533	HepG2	liver:	n/a	n/a
30	CTCF	chr12:9691647-9691785	MCF-7	breast:	n/a	n/a
31	CTCF	chr12:9621713-9621898	Gliobla	brain:	n/a	n/a
32	CTCF	chr12:9621740-9621890	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr12:9691717-9691734	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr12:9631691-9631725	GM20000	blood:	n/a	n/a
35	CTCF	chr12:9621720-9621870	GM12865	blood:	n/a	n/a
36	CTCF	chr12:9621720-9621870	BE2_C	brain:	n/a	n/a
37	CTCF	chr12:9621688-9621907	Pancreas_OC	pancreas:	n/a	n/a
38	CTCF	chr12:9621720-9621870	K562	blood:	n/a	n/a
39	CTCF	chr12:9621720-9621870	HPF	lung:	n/a	n/a
40	CTCF	chr12:9621691-9621911	MCF-7	breast:	n/a	n/a
41	CTCF	chr12:9621760-9621910	HVMF	connective:	n/a	n/a
42	CTCF	chr12:9723279-9723384	GM19238	blood:	n/a	n/a
43	CTCF	chr12:9621715-9621836	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr12:9621681-9621894	ProgFib	skin:	n/a	n/a
45	CTCF	chr12:9725642-9725709	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chr12:9620859-9620943	GM10266	blood:	n/a	chr12:9620903-9620916 chr12:9620900-9620918 chr12:9620902-9620923
47	CTCF	chr12:9620820-9620970	HEEpiC	esophagus:	n/a	chr12:9620903-9620916 chr12:9620900-9620918 chr12:9620902-9620923
48	CTCF	chr12:9665360-9665558	A549	lung:	n/a	n/a
49	CTCF	chr12:9620798-9621051	GM12878	blood:	n/a	chr12:9620903-9620916 chr12:9620900-9620918 chr12:9620902-9620923
50	CTCF	chr12:9621720-9621870	AG04449	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9720554-9720604	SK-N-SH	brain:	n/a
2	chr12:9720554-9720604	SK-N-SH	brain:	n/a
3	chr12:9618783-9618833	MCF10A-Er-Src	breast:	n/a
4	chr12:9720090-9720140	U87	brain:	n/a
5	chr12:9720554-9720604	HRPEpiC	eye:	n/a
6	chr12:9618783-9618833	ovcar-3	ovarian:	n/a
7	chr12:9723402-9723452	CMK	blood:	n/a
8	chr12:9720554-9720604	GM12892	blood:	n/a
9	chr12:9720090-9720140	Jurkat	blood:	n/a
10	chr12:9723402-9723452	AG09319	gingival:	n/a
11	chr12:9722091-9722141	HEK293	kidney:	embryo
12	chr12:9723402-9723452	SK-N-MC	brain:	n/a
13	chr12:9720090-9720140	SK-N-MC	brain:	n/a
14	chr12:9722091-9722141	PANC-1	pancreas:	n/a
15	chr12:9720090-9720140	LNCaP	prostate:	n/a
16	chr12:9720090-9720140	PANC-1	pancreas:	n/a
17	chr12:9722091-9722141	HIPEpiC	eye:	n/a
18	chr12:9720090-9720140	MCF-7	breast:	n/a
19	chr12:9618783-9618833	SAEC	small airway:	n/a
20	chr12:9618783-9618833	PrEC	prostate:	n/a
21	chr12:9720090-9720140	SKMC	muscle:	n/a
22	chr12:9720090-9720140	GM12892	blood:	n/a
23	chr12:9723402-9723452	AG10803	skin:	n/a
24	chr12:9720090-9720140	AG09309	skin:	n/a
25	chr12:9720090-9720140	AG04449	skin:	fetal
26	chr12:9723402-9723452	HAEpiC	amniotic membrane:	n/a
27	chr12:9720554-9720604	NHDF-neo	bronchial:	n/a
28	chr12:9618783-9618833	K562	blood:	n/a
29	chr12:9618783-9618833	HCPEpiC	choroid plexus:	n/a
30	chr12:9618783-9618833	Jurkat	blood:	n/a
31	chr12:9618783-9618833	HRCEpiC	kidney:	n/a
32	chr12:9720554-9720604	AG04449	skin:	fetal
33	chr12:9722091-9722141	PrEC	prostate:	n/a
34	chr12:9618783-9618833	Caco-2	colon:	n/a
35	chr12:9720090-9720140	MCF10A-Er-Src	breast:	n/a
36	chr12:9722091-9722141	HCPEpiC	choroid plexus:	n/a
37	chr12:9722091-9722141	SK-N-MC	brain:	n/a
38	chr12:9722091-9722141	HRCEpiC	kidney:	n/a
39	chr12:9723402-9723452	HRPEpiC	eye:	n/a
40	chr12:9722091-9722141	HCM	heart:	n/a
41	chr12:9618783-9618833	HRE	kidney:	n/a
42	chr12:9720090-9720140	K562	blood:	n/a
43	chr12:9720090-9720140	Hela-S3	cervix:	n/a
44	chr12:9720554-9720604	HEEpiC	esophagus:	n/a
45	chr12:9720090-9720140	ProgFib	skin:	n/a
46	chr12:9723402-9723452	PANC-1	pancreas:	n/a
47	chr12:9618783-9618833	RPTEC	kidney:	n/a
48	chr12:9720090-9720140	HEEpiC	esophagus:	n/a
49	chr12:9723402-9723452	HCPEpiC	choroid plexus:	n/a
50	chr12:9723402-9723452	HIPEpiC	eye:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:9620209..9621328-chr12:31206996..31207808,4	MCF-7	breast:
2	chr12:9620489..9621323-chr12:31206721..31207493,2	MCF-7	breast:
3	chr12:9740551..9742492-chr12:9759137..9760711,2	K562	blood:
4	chr12:9530894..9532008-chr12:9621312..9622244,4	MCF-7	breast:
5	chr12:9739995..9741756-chr12:9800822..9803051,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC2D-9	chr12:9725599-9725666	NONHSAT026830
2	lnc-CLEC2D-9	chr12:9728714-9728863	NONHSAT026830
3	lnc-CLEC2D-2	chr12:9613919-9614245	FPKM1_group_5754_transcript_1
4	lnc-KLRB1-2	chr12:9691704-9691933	l_603_chr12:9690762-9691933_testes
5	lnc-CLEC2D-9	chr12:9724057-9724169	NONHSAT026830
6	lnc-KLRB1-2	chr12:9690763-9691239	l_603_chr12:9690762-9691933_testes
7	lnc-CLEC2D-9	chr12:9725984-9726130	NONHSAT026830
8	lnc-CLEC2D-9	chr12:9728239-9728313	NONHSAT026830
9	lnc-CLEC2D-9	chr12:9723357-9723488	NONHSAT026830
10	lnc-CLEC2D-9	chr12:9727443-9727545	NONHSAT026830
11	lnc-CLEC2D-2	chr12:9613920-9614245	XLOC_009653

No data

Variant related genes	Relation type
ENSG00000266633	TF binding region
ENSG00000256975	TF binding region
ENSG00000214776	TF binding region
ENSG00000266633	CpG island
ENSG00000256975	CpG island
ENSG00000214776	CpG island
ENSG00000111796	chromatin interactions
CALU	miRNA target sites

Extended variants
information (count: 2976 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2976 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs58805431	chr12:9609318-9609319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs375327415	chr12:9609387-9609388	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532240033	chr12:9609388-9609389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545840086	chr12:9609393-9609394	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372330866	chr12:9609520-9609521	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2543222	chr12:9609523-9609524	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182976567	chr12:9609557-9609558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs56884533	chr12:9609578-9609579	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs185237382	chr12:9609596-9609597	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147715532	chr12:9609653-9609654	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs11613428	chr12:9609771-9609772	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs2543219	chr12:9609824-9609825	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568300798	chr12:9609881-9609882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200076774	chr12:9609890-9609891	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs11610951	chr12:9609931-9609932	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs11613003	chr12:9609946-9609947	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
17	rs11613863	chr12:9610031-9610032	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs2536721	chr12:9610070-9610071	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs186946774	chr12:9610108-9610109	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192785005	chr12:9610109-9610110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs72543745	chr12:9610124-9610125	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7976900	chr12:9610125-9610126	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs114827495	chr12:9610172-9610173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138000155	chr12:9610179-9610180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201302038	chr12:9610227-9610228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368386289	chr12:9610228-9610229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs12580010	chr12:9610248-9610249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs117743949	chr12:9610266-9610267	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
29	rs149502751	chr12:9610299-9610300	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
30	rs200522597	chr12:9610316-9610317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs373830543	chr12:9610326-9610327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs115676677	chr12:9610342-9610343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs199997015	chr12:9610352-9610353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372038307	chr12:9610572-9610573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375128465	chr12:9610584-9610585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs60089071	chr12:9610626-9610627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572686491	chr12:9610666-9610667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2536720	chr12:9610711-9610712	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs145639260	chr12:9610765-9610766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10466817	chr12:9610797-9610798	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs2536719	chr12:9610808-9610809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs146429107	chr12:9610854-9610855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545931900	chr12:9610938-9610939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2536717	chr12:9610970-9610971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562543154	chr12:9611058-9611059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184458945	chr12:9611102-9611103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576113464	chr12:9611136-9611137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188987534	chr12:9611152-9611153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145583067	chr12:9611268-9611269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2536715	chr12:9611332-9611333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	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
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21611746	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
small cell lung cancer	20016488	CNVD
Incontinentia Pigmenti	22033527	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Cancer	21272361	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:171 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9607200-9623000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr12:9608200-9610200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr12:9608200-9610200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr12:9608400-9609600	Enhancers	K562	blood
5	chr12:9608800-9642800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr12:9610200-9617000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr12:9610200-9621000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr12:9611200-9621400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr12:9612200-9612600	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr12:9613600-9615400	Enhancers	Primary B cells from peripheral blood	blood
11	chr12:9615000-9615200	Enhancers	Fetal Muscle Leg	muscle
12	chr12:9615200-9621600	Weak transcription	Fetal Muscle Leg	muscle
13	chr12:9615400-9622600	Weak transcription	Primary B cells from peripheral blood	blood
14	chr12:9617000-9618800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr12:9617400-9621600	Weak transcription	Fetal Lung	lung
16	chr12:9617600-9618200	Enhancers	GM12878-XiMat	blood
17	chr12:9617800-9622800	Weak transcription	Primary hematopoietic stem cells	blood
18	chr12:9618200-9622600	Weak transcription	GM12878-XiMat	blood
19	chr12:9618800-9621000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr12:9619600-9621600	Enhancers	Fetal Heart	heart
21	chr12:9619600-9623600	Enhancers	Fetal Thymus	thymus
22	chr12:9620800-9621200	Enhancers	Primary T killer memory cells from peripheral blood	blood
23	chr12:9620800-9623600	Enhancers	Primary T cells from cord blood	blood
24	chr12:9620800-9623600	Enhancers	Primary T cells fromperipheralblood	blood
25	chr12:9621000-9621200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr12:9621000-9621400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr12:9621000-9621600	Enhancers	HSMMtube	muscle
28	chr12:9621000-9621800	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chr12:9621000-9621800	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr12:9621000-9621800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr12:9621000-9621800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr12:9621000-9622000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr12:9621000-9622000	Enhancers	HepG2	liver
34	chr12:9621000-9622200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr12:9621000-9623600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr12:9621200-9621400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr12:9621200-9621800	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr12:9621200-9621800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr12:9621400-9621600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr12:9621400-9621800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr12:9621400-9621800	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr12:9621400-9622000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr12:9621400-9622000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr12:9621400-9622400	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr12:9621400-9623600	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr12:9621600-9621800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr12:9621600-9621800	Enhancers	Fetal Muscle Leg	muscle
48	chr12:9621600-9621800	Enhancers	Thymus	Thymus
49	chr12:9621600-9622000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr12:9621600-9622000	Enhancers	Liver	Liver

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