Variant report

Variant	nsv1048137
Chromosome Location	chr12:60432594-60515455
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:419)
CpG islands
(count:0)
Chromatin interactive
region (count:44)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:419 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:60471816-60472199	K562	blood:	n/a	n/a
2	BHLHE40	chr12:60471887-60471910	GM12878	blood:	n/a	n/a
3	BHLHE40	chr12:60513331-60513358	K562	blood:	n/a	n/a
4	CBX3	chr12:60501770-60502080	K562	blood:	n/a	n/a
5	CEBPB	chr12:60464408-60464802	MCF-7	breast:	n/a	n/a
6	CEBPB	chr12:60487973-60488330	IMR90	lung:	n/a	chr12:60488086-60488097 chr12:60488086-60488099
7	CEBPB	chr12:60505966-60506178	A549	lung:	n/a	n/a
8	CEBPB	chr12:60487941-60488315	Hela-S3	cervix:	n/a	chr12:60488086-60488097 chr12:60488086-60488099
9	CEBPB	chr12:60505870-60506180	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr12:60513111-60513659	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr12:60488079-60488301	A549	lung:	n/a	chr12:60488086-60488097 chr12:60488086-60488099
12	CEBPB	chr12:60505875-60506213	IMR90	lung:	n/a	n/a
13	CEBPB	chr12:60505837-60506241	K562	blood:	n/a	n/a
14	CEBPB	chr12:60500622-60500773	K562	blood:	n/a	n/a
15	CEBPB	chr12:60502756-60503018	K562	blood:	n/a	n/a
16	CEBPB	chr12:60488006-60488199	HepG2	liver:	n/a	chr12:60488086-60488097 chr12:60488086-60488099
17	CEBPB	chr12:60505855-60506196	HepG2	liver:	n/a	n/a
18	CTCF	chr12:60500120-60500270	HMEC	breast:	n/a	n/a
19	CTCF	chr12:60500220-60500370	HBMEC	blood vessel:	n/a	n/a
20	CTCF	chr12:60500140-60500290	NHDF-neo	bronchial:	n/a	n/a
21	CTCF	chr12:60452940-60453090	MCF-7	breast:	n/a	n/a
22	CTCF	chr12:60500080-60500230	AG10803	skin:	n/a	n/a
23	CTCF	chr12:60485716-60485751	Fibrobl	skin:	n/a	n/a
24	CTCF	chr12:60453060-60453210	HCFaa	heart:	n/a	n/a
25	CTCF	chr12:60500240-60500390	WI-38	lung:	n/a	n/a
26	CTCF	chr12:60500040-60500190	HFF-Myc	foreskin:	n/a	n/a
27	CTCF	chr12:60500080-60500230	NHDF-neo	bronchial:	n/a	n/a
28	CTCF	chr12:60500080-60500230	HA-sp	spinal cord:	n/a	n/a
29	CTCF	chr12:60500100-60500250	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr12:60500200-60500350	HAc	cerebellar:	n/a	n/a
31	CTCF	chr12:60500160-60500310	RPTEC	kidney:	n/a	n/a
32	CTCF	chr12:60453040-60453190	NHEK	skin:	n/a	n/a
33	CTCF	chr12:60500142-60500233	HepG2	liver:	n/a	n/a
34	CTCF	chr12:60500100-60500250	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr12:60500120-60500270	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr12:60500140-60500290	K562	blood:	n/a	n/a
37	CTCF	chr12:60500080-60500230	HVMF	connective:	n/a	n/a
38	CTCF	chr12:60500120-60500270	HPF	lung:	n/a	n/a
39	CTCF	chr12:60500080-60500230	HRE	kidney:	n/a	n/a
40	CTCF	chr12:60500120-60500270	AG09309	skin:	n/a	n/a
41	CTCF	chr12:60500140-60500290	HCT-116	colon:	n/a	n/a
42	CTCF	chr12:60500100-60500250	HCFaa	heart:	n/a	n/a
43	CTCF	chr12:60499980-60500130	HCM	heart:	n/a	n/a
44	CTCF	chr12:60500100-60500250	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr12:60500061-60500296	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr12:60453000-60453150	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr12:60453040-60453190	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr12:60500080-60500230	AG04449	skin:	n/a	n/a
49	CTCF	chr12:60471701-60471732	GM13976	blood:	n/a	n/a
50	CTCF	chr12:60506311-60506366	Lung_OC	lung:	n/a	n/a

No data

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:60460447..60462196-chr12:60466989..60469396,2	K562	blood:
2	chr12:60465097..60467873-chr12:60470417..60472937,3	MCF-7	breast:
3	chr12:60463450..60465824-chr12:60478986..60481258,2	MCF-7	breast:
4	chr12:60468174..60469728-chr12:60471025..60473459,2	MCF-7	breast:
5	chr12:60448484..60450647-chr12:60452739..60455616,2	K562	blood:
6	chr12:60466885..60469119-chr12:60493136..60496064,3	MCF-7	breast:
7	chr12:60493772..60496447-chr12:60496844..60499476,2	K562	blood:
8	chr12:60483685..60486608-chr12:60491764..60494624,2	MCF-7	breast:
9	chr12:60463450..60465824-chr12:60478986..60481258,2	MCF-7	breast:
10	chr12:60478315..60480971-chr12:60488037..60490719,3	MCF-7	breast:
11	chr12:60471895..60473733-chr12:60474074..60477071,2	MCF-7	breast:
12	chr12:60442817..60444737-chr12:60445729..60447893,2	K562	blood:
13	chr12:60466885..60469119-chr12:60493136..60496064,3	MCF-7	breast:
14	chr12:60473802..60475803-chr12:60480234..60482937,2	MCF-7	breast:
15	chr12:60499782..60500621-chr12:60887467..60888321,3	MCF-7	breast:
16	chr12:60468174..60469728-chr12:60471025..60473459,2	MCF-7	breast:
17	chr12:60437721..60438429-chr8:43096750..43097250,2	MCF-7	breast:
18	chr12:60461970..60464211-chr12:60465232..60466795,2	MCF-7	breast:
19	chr12:60472741..60475079-chr12:60479250..60481071,2	K562	blood:
20	chr12:60504072..60505898-chr12:60508585..60511528,2	K562	blood:
21	chr12:60483685..60486608-chr12:60491764..60494624,2	MCF-7	breast:
22	chr12:60448484..60450647-chr12:60452739..60455616,2	K562	blood:
23	chr12:60485367..60488154-chr12:60489421..60491431,2	MCF-7	breast:
24	chr12:60454406..60456057-chr12:60465200..60468132,2	MCF-7	breast:
25	chr12:60454406..60456057-chr12:60465200..60468132,2	MCF-7	breast:
26	chr12:60465097..60467873-chr12:60470417..60472937,3	MCF-7	breast:
27	chr12:60466814..60469463-chr12:60479017..60481348,2	MCF-7	breast:
28	chr12:60459856..60461380-chr12:60466711..60469397,2	MCF-7	breast:
29	chr12:60460447..60462196-chr12:60466989..60469396,2	K562	blood:
30	chr12:60493772..60496447-chr12:60496844..60499476,2	K562	blood:
31	chr12:60461970..60464211-chr12:60465232..60466795,2	MCF-7	breast:
32	chr12:60439937..60442180-chr12:60446699..60448272,2	MCF-7	breast:
33	chr12:60504072..60505898-chr12:60508585..60511528,2	K562	blood:
34	chr12:60442817..60444737-chr12:60445729..60447893,2	K562	blood:
35	chr12:60439937..60442180-chr12:60446699..60448272,2	MCF-7	breast:
36	chr12:60473802..60475803-chr12:60480234..60482937,2	MCF-7	breast:
37	chr12:60464696..60468583-chr12:60490353..60494821,4	MCF-7	breast:
38	chr12:60472741..60475079-chr12:60479250..60481071,2	K562	blood:
39	chr12:60478315..60480971-chr12:60488037..60490719,3	MCF-7	breast:
40	chr12:60481263..60483527-chr12:60485827..60488653,2	K562	blood:
41	chr12:60471895..60473733-chr12:60474074..60477071,2	MCF-7	breast:
42	chr12:60459856..60461380-chr12:60466711..60469397,2	MCF-7	breast:
43	chr12:60466814..60469463-chr12:60479017..60481348,2	MCF-7	breast:
44	chr12:60464696..60468583-chr12:60490353..60494821,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC16A7-2	chr12:60488910-60489632	ENSG00000257294
2	lnc-SLC16A7-2	chr12:60486645-60486690	ENSG00000257294

No data

Variant related genes	Relation type
ENSG00000257294	TF binding region
ENSG00000257294	chromatin interactions

Extended variants
information (count: 1961 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1961 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538539133	chr12:60436600-60436601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs558564383	chr12:60436612-60436613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs527374261	chr12:60436617-60436618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572084038	chr12:60436643-60436644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187904197	chr12:60436649-60436650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs561188019	chr12:60436688-60436689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138903248	chr12:60436698-60436699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs142813778	chr12:60436758-60436759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs78384085	chr12:60436761-60436762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs547557285	chr12:60436805-60436806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567269566	chr12:60436838-60436839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs192483853	chr12:60436880-60436881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532895455	chr12:60436921-60436922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs534031875	chr12:60436930-60436931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552883130	chr12:60436971-60436972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs542881489	chr12:60436975-60436976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs146979655	chr12:60437049-60437050	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs549812523	chr12:60437055-60437056	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs113996575	chr12:60437170-60437171	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs116421970	chr12:60437196-60437197	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs567205421	chr12:60437211-60437212	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs529796485	chr12:60437274-60437275	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs549752158	chr12:60437359-60437360	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs569502083	chr12:60437397-60437398	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs538572051	chr12:60437421-60437422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs538948665	chr12:60437446-60437447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs115875688	chr12:60437515-60437516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs4539369	chr12:60437535-60437536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs183772016	chr12:60437537-60437538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs147670534	chr12:60437592-60437593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs116944018	chr12:60437643-60437644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534782355	chr12:60437680-60437681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs371716421	chr12:60437794-60437795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs199730606	chr12:60437803-60437804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555048664	chr12:60437854-60437855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs574882211	chr12:60437866-60437867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs138042512	chr12:60437968-60437969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs113081731	chr12:60437990-60437991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs577486977	chr12:60437998-60437999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546536127	chr12:60438027-60438028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs370501555	chr12:60438091-60438092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560046987	chr12:60438101-60438102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554688891	chr12:60438192-60438193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149483442	chr12:60438236-60438237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540719086	chr12:60438301-60438302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560932883	chr12:60438312-60438313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs117492730	chr12:60438357-60438358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549828333	chr12:60438428-60438429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs12578393	chr12:60438436-60438437	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs17652271	chr12:60438447-60438448	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:83)

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
Renal cell carcinoma	18194544	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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:60436600-60437000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr12:60436800-60437000	Enhancers	HUVEC	blood vessel
3	chr12:60437000-60437400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr12:60437000-60438000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr12:60437000-60442400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:60437200-60437600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr12:60437400-60437800	Enhancers	HUVEC	blood vessel
8	chr12:60437400-60438000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr12:60453800-60454600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr12:60454000-60454600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr12:60454000-60454600	Enhancers	NHEK	skin
12	chr12:60454200-60454400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr12:60454400-60464000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr12:60455600-60456000	Enhancers	Fetal Intestine Small	intestine
15	chr12:60464000-60464200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr12:60464000-60464200	Enhancers	HMEC	breast
17	chr12:60464000-60464600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr12:60464000-60467400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr12:60464000-60467400	Enhancers	NHEK	skin
20	chr12:60464200-60465200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr12:60464200-60465200	Weak transcription	HMEC	breast
22	chr12:60464200-60466800	Enhancers	HUVEC	blood vessel
23	chr12:60464400-60464600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr12:60464400-60464600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr12:60464600-60465000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr12:60464600-60465600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr12:60465000-60466200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr12:60465000-60467400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr12:60465200-60465800	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr12:60465200-60467000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr12:60465200-60467000	Enhancers	HMEC	breast
32	chr12:60465600-60467000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr12:60465800-60467600	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr12:60466000-60466400	Enhancers	Aorta	Aorta
35	chr12:60466000-60467400	Enhancers	NH-A	brain
36	chr12:60466200-60467400	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr12:60466200-60467400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr12:60466400-60467000	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr12:60466400-60467600	Enhancers	Fetal Heart	heart
40	chr12:60466600-60467000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr12:60466600-60467400	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr12:60466600-60467400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr12:60466600-60468200	Enhancers	NHDF-Ad	bronchial
44	chr12:60467000-60467400	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr12:60467000-60467400	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr12:60467000-60475200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr12:60467400-60469000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr12:60467600-60471800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr12:60467800-60468200	Enhancers	Fetal Muscle Leg	muscle
50	chr12:60469000-60469200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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