Variant report

Variant	esv1823386
Chromosome Location	chr12:9605283-9716126
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:535)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:535 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

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	ATF3	chr12:9608285-9608446	K562	blood:	n/a	n/a
3	BATF	chr12:9627071-9627414	GM12878	blood:	n/a	chr12:9627229-9627240
4	BATF	chr12:9627069-9627370	GM12878	blood:	n/a	chr12:9627229-9627240
5	BATF	chr12:9623145-9623344	GM12878	blood:	n/a	n/a
6	BHLHE40	chr12:9608196-9608405	K562	blood:	n/a	n/a
7	BHLHE40	chr12:9621680-9621866	K562	blood:	n/a	n/a
8	BRCA1	chr12:9621725-9621746	GM12878	blood:	n/a	n/a
9	CEBPB	chr12:9621651-9621793	HepG2	liver:	n/a	n/a
10	CEBPB	chr12:9621719-9621810	K562	blood:	n/a	n/a
11	CEBPB	chr12:9621705-9621858	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr12:9626831-9627127	Hela-S3	cervix:	n/a	chr12:9626967-9626978
13	CEBPB	chr12:9626847-9627088	A549	lung:	n/a	chr12:9626967-9626978
14	CEBPB	chr12:9626941-9627031	K562	blood:	n/a	chr12:9626967-9626978
15	CEBPB	chr12:9646117-9646284	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr12:9635038-9635326	IMR90	lung:	n/a	chr12:9635144-9635153 chr12:9635144-9635153 chr12:9635144-9635153
17	CEBPB	chr12:9621557-9621862	HepG2	liver:	n/a	n/a
18	CEBPB	chr12:9626864-9627128	K562	blood:	n/a	chr12:9626967-9626978
19	CEBPB	chr12:9626823-9627139	HepG2	liver:	n/a	chr12:9626967-9626978
20	CEBPB	chr12:9699973-9700136	IMR90	lung:	n/a	n/a
21	CEBPB	chr12:9699995-9700109	A549	lung:	n/a	n/a
22	CTCF	chr12:9621668-9621940	K562	blood:	n/a	chr12:9621901-9621914
23	CTCF	chr12:9621700-9621850	GM12868	blood:	n/a	n/a
24	CTCF	chr12:9621720-9621870	HEEpiC	esophagus:	n/a	n/a
25	CTCF	chr12:9621720-9621870	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr12:9621673-9621926	MCF-7	breast:	n/a	chr12:9621901-9621914
27	CTCF	chr12:9665305-9665671	A549	lung:	n/a	n/a
28	CTCF	chr12:9620740-9620890	NHEK	skin:	n/a	n/a
29	CTCF	chr12:9621672-9621919	A549	lung:	n/a	chr12:9621901-9621914
30	CTCF	chr12:9621720-9621870	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr12:9691655-9691786	MCF-7	breast:	n/a	n/a
32	CTCF	chr12:9621697-9621947	HUVEC	blood vessel:	n/a	chr12:9621901-9621914
33	CTCF	chr12:9665444-9665629	K562	blood:	n/a	n/a
34	CTCF	chr12:9620840-9620990	HMF	breast:	n/a	chr12:9620903-9620916 chr12:9620900-9620918 chr12:9620902-9620923
35	CTCF	chr12:9621720-9621870	NHDF-neo	bronchial:	n/a	n/a
36	CTCF	chr12:9620840-9620990	AG10803	skin:	n/a	chr12:9620903-9620916 chr12:9620900-9620918 chr12:9620902-9620923
37	CTCF	chr12:9621720-9621870	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr12:9621740-9621890	GM12874	blood:	n/a	n/a
39	CTCF	chr12:9621720-9621870	GM12867	blood:	n/a	n/a
40	CTCF	chr12:9621760-9621910	GM12878	blood:	n/a	n/a
41	CTCF	chr12:9620820-9620970	AG10803	skin:	n/a	chr12:9620903-9620916 chr12:9620900-9620918 chr12:9620902-9620923
42	CTCF	chr12:9621540-9621690	SAEC	small airway:	n/a	n/a
43	CTCF	chr12:9620800-9620950	HPAF	blood vessel:	n/a	chr12:9620903-9620916 chr12:9620900-9620918 chr12:9620902-9620923
44	CTCF	chr12:9621734-9621904	GM10248	blood:	n/a	n/a
45	CTCF	chr12:9621688-9621907	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr12:9621672-9621908	MCF-7	breast:	n/a	n/a
47	CTCF	chr12:9703380-9703388	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr12:9621740-9621890	GM12870	blood:	n/a	n/a
49	CTCF	chr12:9611583-9611589	GM10248	blood:	n/a	n/a
50	CTCF	chr12:9620814-9620966	HepG2	liver:	n/a	chr12:9620903-9620916 chr12:9620900-9620918 chr12:9620902-9620923

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9618783-9618833	PANC-1	pancreas:	n/a
2	chr12:9618783-9618833	GM12878	blood:	n/a
3	chr12:9618783-9618833	IMR90	lung:	fetal
4	chr12:9618783-9618833	SK-N-SH_RA	brain:	n/a
5	chr12:9618783-9618833	HCPEpiC	choroid plexus:	n/a
6	chr12:9618783-9618833	U87	brain:	n/a
7	chr12:9618783-9618833	Hepatocyte	liver:	n/a
8	chr12:9618783-9618833	MCF-7	breast:	n/a
9	chr12:9618783-9618833	MCF10A-Er-Src	breast:	n/a
10	chr12:9618783-9618833	HRCEpiC	kidney:	n/a
11	chr12:9618783-9618833	NB4	blood:	n/a
12	chr12:9618783-9618833	A549	lung:	n/a
13	chr12:9618783-9618833	HRPEpiC	eye:	n/a
14	chr12:9618783-9618833	BE2_C	brain:	n/a
15	chr12:9618783-9618833	HCF	heart:	n/a
16	chr12:9618783-9618833	AG10803	skin:	n/a
17	chr12:9618783-9618833	SAEC	small airway:	n/a
18	chr12:9618783-9618833	Caco-2	colon:	n/a
19	chr12:9618783-9618833	HUVEC	blood vessel:	n/a
20	chr12:9618783-9618833	Hela-S3	cervix:	n/a
21	chr12:9618783-9618833	HL-60	blood:	n/a
22	chr12:9618783-9618833	T-47D	breast:	n/a
23	chr12:9618783-9618833	PrEC	prostate:	n/a
24	chr12:9618783-9618833	AG04450	lung:	fetal
25	chr12:9618783-9618833	HPAEpiC	pulmonary alveolar:	n/a
26	chr12:9618783-9618833	HRE	kidney:	n/a
27	chr12:9618783-9618833	SK-N-SH	brain:	n/a
28	chr12:9618783-9618833	H1-hESC	embryonic stem cell:	embryo
29	chr12:9618783-9618833	HIPEpiC	eye:	n/a
30	chr12:9618783-9618833	HAEpiC	amniotic membrane:	n/a
31	chr12:9618783-9618833	ECC-1	luminal epithelium:	n/a
32	chr12:9618783-9618833	NH-A	brain:	n/a
33	chr12:9618783-9618833	SKMC	muscle:	n/a
34	chr12:9618783-9618833	BJ	skin:	n/a
35	chr12:9618783-9618833	HEEpiC	esophagus:	n/a
36	chr12:9618783-9618833	PFSK-1	brain:	n/a
37	chr12:9618783-9618833	NHDF-neo	bronchial:	n/a
38	chr12:9618783-9618833	ovcar-3	ovarian:	n/a
39	chr12:9618783-9618833	RPTEC	kidney:	n/a
40	chr12:9618783-9618833	SK-N-MC	brain:	n/a
41	chr12:9618783-9618833	GM06990	blood:	n/a
42	chr12:9618783-9618833	HNPCEpiC	eye:	n/a
43	chr12:9618783-9618833	HepG2	liver:	n/a
44	chr12:9618783-9618833	HCM	heart:	n/a
45	chr12:9618783-9618833	NHBE	bronchial:	n/a
46	chr12:9618783-9618833	AG09319	gingival:	n/a
47	chr12:9618783-9618833	ProgFib	skin:	n/a
48	chr12:9618783-9618833	LNCaP	prostate:	n/a
49	chr12:9618783-9618833	AG04449	skin:	fetal
50	chr12:9618783-9618833	GM19239	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:9530894..9532008-chr12:9621312..9622244,4	MCF-7	breast:
2	chr12:9620489..9621323-chr12:31206721..31207493,2	MCF-7	breast:
3	chr12:9620209..9621328-chr12:31206996..31207808,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC2D-2	chr12:9613920-9614245	XLOC_009653
2	lnc-CLEC2D-2	chr12:9613919-9614245	FPKM1_group_5754_transcript_1
3	lnc-KLRB1-2	chr12:9691704-9691933	l_603_chr12:9690762-9691933_testes
4	lnc-KLRB1-2	chr12:9690763-9691239	l_603_chr12:9690762-9691933_testes

No data

Variant related genes	Relation type
DDX12P	TF binding region
ENSG00000266633	TF binding region
ENSG00000256975	TF binding region
ENSG00000214776	TF binding region
DDX12P	CpG island
ENSG00000266633	CpG island
ENSG00000256975	CpG island
ENSG00000214776	CpG island
CALU	miRNA target sites

Extended variants
information (count: 2193 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2193 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28545519	chr12:9605283-9605284	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs142595682	chr12:9605316-9605317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs111262397	chr12:9605338-9605339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs117821888	chr12:9605377-9605378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372889970	chr12:9605438-9605439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187192247	chr12:9605443-9605444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs375603540	chr12:9605501-9605502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs145024182	chr12:9605553-9605554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs199687219	chr12:9605602-9605603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs192122426	chr12:9605613-9605614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs183849295	chr12:9605619-9605620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs146783554	chr12:9605713-9605714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs74240357	chr12:9605733-9605734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs140733631	chr12:9605806-9605807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs2536730	chr12:9605817-9605818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145908133	chr12:9605864-9605865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374244569	chr12:9605876-9605877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2543238	chr12:9605920-9605921	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
19	rs546608511	chr12:9605949-9605950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs397829870	chr12:9605956-9605957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201716316	chr12:9605985-9605986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs76820849	chr12:9605987-9605988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs138458077	chr12:9606082-9606083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10843826	chr12:9606106-9606107	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
25	rs569959596	chr12:9606108-9606109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10082986	chr12:9606109-9606110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs58028294	chr12:9606145-9606146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149616636	chr12:9606165-9606166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569129520	chr12:9606203-9606204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538075890	chr12:9606252-9606253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs10082891	chr12:9606269-9606270	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs577683822	chr12:9606304-9606305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs141677360	chr12:9606320-9606321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs57055518	chr12:9606342-9606343	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs188624027	chr12:9606366-9606367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs534022434	chr12:9606412-9606413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192639310	chr12:9606418-9606419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs4763320	chr12:9606435-9606436	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs10082989	chr12:9606440-9606441	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs147433929	chr12:9606605-9606606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs139175929	chr12:9606607-9606608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201449963	chr12:9606644-9606645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12579943	chr12:9606720-9606721	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs190597307	chr12:9606755-9606756	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs149943508	chr12:9606787-9606788	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144996215	chr12:9606793-9606794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs61915861	chr12:9606803-9606804	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143675042	chr12:9606805-9606806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182325812	chr12:9606833-9606834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs144778219	chr12:9606863-9606864	Enhancers 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:168 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9601800-9606800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr12:9602000-9606800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr12:9602200-9606600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr12:9602200-9606800	Weak transcription	Fetal Heart	heart
5	chr12:9602200-9608000	Weak transcription	HUVEC	blood vessel
6	chr12:9602400-9605600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr12:9602400-9606400	Weak transcription	NHEK	skin
8	chr12:9602400-9606600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr12:9602400-9606600	Weak transcription	K562	blood
10	chr12:9603400-9606400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr12:9603800-9606600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr12:9604000-9606600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr12:9605600-9605800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr12:9605800-9606200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr12:9606200-9607400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr12:9606400-9607200	Enhancers	NHEK	skin
17	chr12:9606400-9607600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr12:9606600-9607000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr12:9606600-9607200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr12:9606600-9607200	Enhancers	K562	blood
21	chr12:9606600-9607800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr12:9606600-9607800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr12:9606800-9607200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr12:9606800-9607200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr12:9606800-9608800	Enhancers	Fetal Heart	heart
26	chr12:9607000-9608200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr12:9607200-9608200	Weak transcription	NHEK	skin
28	chr12:9607200-9608400	Weak transcription	K562	blood
29	chr12:9607200-9623000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr12:9607400-9608200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr12:9607800-9608200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr12:9607800-9608200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr12:9608000-9608200	Weak transcription	Spleen	Spleen
34	chr12:9608000-9609000	Enhancers	HUVEC	blood vessel
35	chr12:9608200-9608400	Enhancers	Spleen	Spleen
36	chr12:9608200-9608400	Enhancers	HMEC	breast
37	chr12:9608200-9608600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr12:9608200-9608800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr12:9608200-9608800	Enhancers	NHEK	skin
40	chr12:9608200-9610200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr12:9608200-9610200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr12:9608400-9609600	Enhancers	K562	blood
43	chr12:9608800-9642800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr12:9610200-9617000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr12:9610200-9621000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr12:9611200-9621400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr12:9612200-9612600	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr12:9613600-9615400	Enhancers	Primary B cells from peripheral blood	blood
49	chr12:9615000-9615200	Enhancers	Fetal Muscle Leg	muscle
50	chr12:9615200-9621600	Weak transcription	Fetal Muscle Leg	muscle

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