Variant report

Variant	nsv898753
Chromosome Location	chr12:9644018-9755578
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:261)
CpG islands
(count:244)
Chromatin interactive
region (count:2)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:261 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:9743025-9743373	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:9740655-9741170	K562	blood:	n/a	n/a
3	ARID3A	chr12:9741257-9741854	HepG2	liver:	n/a	n/a
4	ATF1	chr12:9740572-9740926	K562	blood:	n/a	n/a
5	BACH1	chr12:9740595-9741065	K562	blood:	n/a	n/a
6	BACH1	chr12:9740652-9740897	H1-hESC	embryonic stem cell:	n/a	n/a
7	CCNT2	chr12:9740427-9741071	K562	blood:	n/a	n/a
8	CEBPB	chr12:9699973-9700136	IMR90	lung:	n/a	n/a
9	CEBPB	chr12:9646117-9646284	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr12:9741394-9741705	HepG2	liver:	n/a	n/a
11	CEBPB	chr12:9728216-9728457	A549	lung:	n/a	n/a
12	CEBPB	chr12:9699995-9700109	A549	lung:	n/a	n/a
13	CEBPZ	chr12:9741497-9741533	HepG2	liver:	n/a	n/a
14	CTCF	chr12:9665458-9665601	Kidney_OC	kidney:	n/a	n/a
15	CTCF	chr12:9665374-9665581	MCF-7	breast:	n/a	n/a
16	CTCF	chr12:9709315-9709383	LNCaP	prostate:	n/a	n/a
17	CTCF	chr12:9725642-9725709	Spleen_OC	spleen:	n/a	n/a
18	CTCF	chr12:9665435-9665535	MCF-7	breast:	n/a	n/a
19	CTCF	chr12:9665390-9665555	ProgFib	skin:	n/a	n/a
20	CTCF	chr12:9726760-9726829	Spleen_OC	spleen:	n/a	n/a
21	CTCF	chr12:9695383-9695441	GM20000	blood:	n/a	n/a
22	CTCF	chr12:9665459-9665498	Fibrobl	skin:	n/a	n/a
23	CTCF	chr12:9665411-9665564	GM10248	blood:	n/a	n/a
24	CTCF	chr12:9665444-9665629	K562	blood:	n/a	n/a
25	CTCF	chr12:9695807-9695847	GM13976	blood:	n/a	n/a
26	CTCF	chr12:9665360-9665510	HEEpiC	esophagus:	n/a	n/a
27	CTCF	chr12:9669822-9669862	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr12:9724378-9724451	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr12:9665360-9665590	MCF-7	breast:	n/a	n/a
30	CTCF	chr12:9736624-9736653	Pancreas_OC	pancreas:	n/a	n/a
31	CTCF	chr12:9723300-9723450	HA-sp	spinal cord:	n/a	n/a
32	CTCF	chr12:9665389-9665592	LNCaP	prostate:	n/a	n/a
33	CTCF	chr12:9665305-9665671	A549	lung:	n/a	n/a
34	CTCF	chr12:9691655-9691786	MCF-7	breast:	n/a	n/a
35	CTCF	chr12:9730398-9730556	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr12:9665431-9665574	Medullo	brain:	n/a	n/a
37	CTCF	chr12:9719543-9719625	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr12:9665294-9665690	A549	lung:	n/a	n/a
39	CTCF	chr12:9665383-9665586	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr12:9665406-9665624	Pancreas_OC	pancreas:	n/a	n/a
41	CTCF	chr12:9665377-9665602	K562	blood:	n/a	n/a
42	CTCF	chr12:9665352-9665595	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr12:9665369-9665585	GM13976	blood:	n/a	n/a
44	CTCF	chr12:9665424-9665591	GM10266	blood:	n/a	n/a
45	CTCF	chr12:9665376-9665490	HepG2	liver:	n/a	n/a
46	CTCF	chr12:9730389-9730511	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr12:9665402-9665599	LNCaP	prostate:	n/a	n/a
48	CTCF	chr12:9691647-9691785	MCF-7	breast:	n/a	n/a
49	CTCF	chr12:9665359-9665586	Gliobla	brain:	n/a	n/a
50	CTCF	chr12:9697887-9697942	GM13977	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9720554-9720604	NH-A	brain:	n/a
2	chr12:9720090-9720140	GM12891	blood:	n/a
3	chr12:9722091-9722141	NHDF-neo	bronchial:	n/a
4	chr12:9720090-9720140	NHDF-neo	bronchial:	n/a
5	chr12:9720554-9720604	AG09319	gingival:	n/a
6	chr12:9720554-9720604	AG09309	skin:	n/a
7	chr12:9722091-9722141	RPTEC	kidney:	n/a
8	chr12:9720554-9720604	NT2-D1	testis:	n/a
9	chr12:9722091-9722141	HMEC	breast:	n/a
10	chr12:9723402-9723452	BE2_C	brain:	n/a
11	chr12:9723402-9723452	PANC-1	pancreas:	n/a
12	chr12:9720090-9720140	HRCEpiC	kidney:	n/a
13	chr12:9720090-9720140	GM12892	blood:	n/a
14	chr12:9723402-9723452	SAEC	small airway:	n/a
15	chr12:9720554-9720604	SKMC	muscle:	n/a
16	chr12:9723402-9723452	NHBE	bronchial:	n/a
17	chr12:9723402-9723452	HAEpiC	amniotic membrane:	n/a
18	chr12:9722091-9722141	SK-N-SH_RA	brain:	n/a
19	chr12:9720090-9720140	HUVEC	blood vessel:	n/a
20	chr12:9723402-9723452	MCF10A-Er-Src	breast:	n/a
21	chr12:9722091-9722141	HCF	heart:	n/a
22	chr12:9720090-9720140	HIPEpiC	eye:	n/a
23	chr12:9720554-9720604	Caco-2	colon:	n/a
24	chr12:9722091-9722141	Jurkat	blood:	n/a
25	chr12:9720554-9720604	IMR90	lung:	fetal
26	chr12:9720554-9720604	MCF10A-Er-Src	breast:	n/a
27	chr12:9720554-9720604	ECC-1	luminal epithelium:	n/a
28	chr12:9722091-9722141	HCM	heart:	n/a
29	chr12:9720554-9720604	AG04449	skin:	fetal
30	chr12:9723402-9723452	HMEC	breast:	n/a
31	chr12:9722091-9722141	LNCaP	prostate:	n/a
32	chr12:9723402-9723452	T-47D	breast:	n/a
33	chr12:9720554-9720604	GM12892	blood:	n/a
34	chr12:9720090-9720140	A549	lung:	n/a
35	chr12:9720090-9720140	HAEpiC	amniotic membrane:	n/a
36	chr12:9720090-9720140	SK-N-SH	brain:	n/a
37	chr12:9720554-9720604	HUVEC	blood vessel:	n/a
38	chr12:9720554-9720604	NB4	blood:	n/a
39	chr12:9722091-9722141	GM06990	blood:	n/a
40	chr12:9720554-9720604	CMK	blood:	n/a
41	chr12:9720554-9720604	T-47D	breast:	n/a
42	chr12:9720090-9720140	NT2-D1	testis:	n/a
43	chr12:9722091-9722141	NH-A	brain:	n/a
44	chr12:9720090-9720140	Hepatocyte	liver:	n/a
45	chr12:9720554-9720604	RPTEC	kidney:	n/a
46	chr12:9720554-9720604	Jurkat	blood:	n/a
47	chr12:9720554-9720604	SK-N-SH	brain:	n/a
48	chr12:9723402-9723452	H1-hESC	embryonic stem cell:	embryo
49	chr12:9722091-9722141	PANC-1	pancreas:	n/a
50	chr12:9720090-9720140	AG09319	gingival:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:9739995..9741756-chr12:9800822..9803051,2	K562	blood:
2	chr12:9740551..9742492-chr12:9759137..9760711,2	K562	blood:

(count:9 , 50 per page) page: 1

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

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

Extended variants
information (count: 2420 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2420 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7358735	chr12:9644018-9644019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs183973122	chr12:9644057-9644058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188306054	chr12:9644059-9644060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs180774626	chr12:9644117-9644118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370470799	chr12:9644140-9644141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186372464	chr12:9644197-9644198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs557669353	chr12:9644228-9644229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190260816	chr12:9644243-9644244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs182023342	chr12:9644284-9644285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs148764366	chr12:9644401-9644402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150819846	chr12:9644654-9644655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186559527	chr12:9644725-9644726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs191843277	chr12:9644747-9644748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs201716475	chr12:9644860-9644861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182821148	chr12:9644862-9644863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185648371	chr12:9644871-9644872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189963012	chr12:9644903-9644904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs113565374	chr12:9644994-9644995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182165634	chr12:9645020-9645021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189116188	chr12:9645179-9645180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs193019742	chr12:9645221-9645222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556861607	chr12:9645249-9645250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183690113	chr12:9645400-9645401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188559484	chr12:9645467-9645468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs573745925	chr12:9645485-9645486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192049092	chr12:9645581-9645582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs199851209	chr12:9645640-9645641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs2536640	chr12:9645656-9645657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs74062867	chr12:9645671-9645672	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs2536639	chr12:9645704-9645705	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs542777555	chr12:9645761-9645762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147601043	chr12:9645795-9645796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2638956	chr12:9645842-9645843	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs2536638	chr12:9645893-9645894	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs184105312	chr12:9645925-9645926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2536637	chr12:9645992-9645993	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs140056597	chr12:9646047-9646048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188450532	chr12:9646126-9646127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2575253	chr12:9646128-9646129	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs191353264	chr12:9646284-9646285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs138080172	chr12:9646424-9646425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184158872	chr12:9646427-9646428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190656738	chr12:9646428-9646429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182340599	chr12:9646485-9646486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs28534034	chr12:9646532-9646533	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs4015221	chr12:9646598-9646599	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs190131415	chr12:9646685-9646686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181531215	chr12:9646700-9646701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185788143	chr12:9646799-9646800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368844634	chr12:9646824-9646825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9623200-9653000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr12:9627000-9663400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr12:9655400-9656000	Enhancers	Dnd41	blood
4	chr12:9657000-9664800	Weak transcription	Fetal Lung	lung
5	chr12:9659400-9662200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr12:9661800-9663000	Enhancers	Hela-S3	cervix
7	chr12:9662000-9662800	Enhancers	HMEC	breast
8	chr12:9662000-9663400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr12:9662200-9662600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr12:9662200-9663000	Enhancers	NHEK	skin
11	chr12:9662200-9663400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr12:9662400-9662800	Enhancers	HUVEC	blood vessel
13	chr12:9662400-9663000	Enhancers	Osteobl	bone
14	chr12:9662400-9663400	Enhancers	Fetal Heart	heart
15	chr12:9662600-9663000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr12:9662600-9663200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr12:9662600-9663200	Enhancers	Primary B cells from cord blood	blood
18	chr12:9662600-9664400	Enhancers	Fetal Thymus	thymus
19	chr12:9663000-9663600	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr12:9663000-9664200	Enhancers	Thymus	Thymus
21	chr12:9663400-9663600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr12:9663400-9667200	Weak transcription	Fetal Heart	heart
23	chr12:9663600-9664000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr12:9664000-9664200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr12:9664200-9702200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr12:9665000-9667800	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr12:9667200-9668000	Enhancers	Fetal Heart	heart
28	chr12:9667800-9668600	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr12:9667800-9668800	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr12:9668200-9668800	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr12:9668800-9679600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr12:9679600-9680000	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr12:9686000-9703600	Weak transcription	Hela-S3	cervix
34	chr12:9703600-9705600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr12:9704000-9721800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr12:9705600-9706400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr12:9706400-9735000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr12:9717000-9717400	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr12:9721200-9722400	Weak transcription	Thymus	Thymus
40	chr12:9721400-9723400	Active TSS	Breast Myoepithelial Primary Cells	Breast
41	chr12:9721800-9722000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr12:9721800-9722200	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
43	chr12:9721800-9723000	Active TSS	Right Ventricle	heart
44	chr12:9722000-9723000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr12:9722000-9723000	ZNF genes & repeats	Fetal Thymus	thymus
46	chr12:9722200-9722400	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
47	chr12:9722200-9722800	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr12:9722400-9722600	Active TSS	Fetal Muscle Leg	muscle
49	chr12:9722400-9722800	Active TSS	Sigmoid Colon	Sigmoid Colon
50	chr12:9722400-9723000	Active TSS	Thymus	Thymus

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