Variant report

Variant	nsv557704
Chromosome Location	chr12:20842041-20893980
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr12:20879678-20879846	A549	lung:	n/a	n/a
2	CEBPB	chr12:20854747-20854901	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr12:20874462-20874604	HepG2	liver:	n/a	chr12:20874519-20874530
4	CEBPB	chr12:20874505-20874583	A549	lung:	n/a	chr12:20874519-20874530
5	CEBPB	chr12:20868114-20868299	HepG2	liver:	n/a	chr12:20868231-20868242
6	CTCF	chr12:20868954-20869163	HepG2	liver:	n/a	chr12:20869090-20869108
7	CTCF	chr12:20869000-20869150	HCT-116	colon:	n/a	chr12:20869090-20869108
8	CTCF	chr12:20868960-20869110	HCT-116	colon:	n/a	chr12:20869090-20869108
9	CTCF	chr12:20869016-20869144	MCF-7	breast:	n/a	chr12:20869090-20869108
10	CTCF	chr12:20869040-20869190	BE2_C	brain:	n/a	chr12:20869090-20869108
11	CTCF	chr12:20869030-20869148	Hela-S3	cervix:	n/a	chr12:20869090-20869108
12	CTCF	chr12:20868855-20869208	A549	lung:	n/a	chr12:20869090-20869108
13	CTCF	chr12:20869000-20869150	A549	lung:	n/a	chr12:20869090-20869108
14	CTCF	chr12:20869100-20869250	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr12:20884280-20884430	HPAF	blood vessel:	n/a	chr12:20884367-20884388 chr12:20884365-20884383
16	CTCF	chr12:20884313-20884483	Medullo	brain:	n/a	chr12:20884367-20884388 chr12:20884365-20884383
17	CTCF	chr12:20869100-20869250	HepG2	liver:	n/a	n/a
18	CTCF	chr12:20869020-20869170	Caco-2	colon:	n/a	chr12:20869090-20869108
19	CTCF	chr12:20868980-20869130	WERI-Rb-1	eye:	n/a	chr12:20869090-20869108
20	CTCF	chr12:20869036-20869122	Medullo	brain:	n/a	chr12:20869090-20869108
21	CTCF	chr12:20869032-20869154	HUVEC	blood vessel:	n/a	chr12:20869090-20869108
22	CTCF	chr12:20869011-20869138	A549	lung:	n/a	chr12:20869090-20869108
23	CTCF	chr12:20868952-20869252	H1-hESC	embryonic stem cell:	n/a	chr12:20869090-20869108
24	CTCF	chr12:20868920-20869070	GM12866	blood:	n/a	n/a
25	CTCF	chr12:20884322-20884469	HUVEC	blood vessel:	n/a	chr12:20884367-20884388 chr12:20884365-20884383
26	CTCF	chr12:20869035-20869130	H1-hESC	embryonic stem cell:	n/a	chr12:20869090-20869108
27	CTCF	chr12:20868878-20869202	H1-hESC	embryonic stem cell:	n/a	chr12:20869090-20869108
28	CTCF	chr12:20869059-20869094	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr12:20869020-20869170	GM12865	blood:	n/a	chr12:20869090-20869108
30	CTCF	chr12:20868960-20869110	BE2_C	brain:	n/a	chr12:20869090-20869108
31	CTCF	chr12:20869000-20869150	WERI-Rb-1	eye:	n/a	chr12:20869090-20869108
32	CTCF	chr12:20869180-20869330	BE2_C	brain:	n/a	n/a
33	CTCF	chr12:20891500-20891650	Caco-2	colon:	n/a	n/a
34	CTCF	chr12:20869067-20869145	Gliobla	brain:	n/a	chr12:20869090-20869108
35	CTCF	chr12:20869040-20869190	Caco-2	colon:	n/a	chr12:20869090-20869108
36	CTCF	chr12:20868911-20869245	HepG2	liver:	n/a	chr12:20869090-20869108
37	CTCF	chr12:20884299-20884385	LNCaP	prostate:	n/a	chr12:20884365-20884383
38	CTCF	chr12:20884340-20884490	HRE	kidney:	n/a	chr12:20884367-20884388 chr12:20884365-20884383
39	CTCF	chr12:20869020-20869170	SK-N-SH_RA	brain:	n/a	chr12:20869090-20869108
40	CTCF	chr12:20868972-20869202	A549	lung:	n/a	chr12:20869090-20869108
41	CTCF	chr12:20868980-20869130	HEK293	kidney:	n/a	chr12:20869090-20869108
42	CTCF	chr12:20868982-20869167	A549	lung:	n/a	chr12:20869090-20869108
43	CTCF	chr12:20869120-20869270	NB4	blood:	n/a	n/a
44	CTCF	chr12:20869040-20869190	GM12878	blood:	n/a	chr12:20869090-20869108
45	CTCF	chr12:20869040-20869190	HPAF	blood vessel:	n/a	chr12:20869090-20869108
46	CTCF	chr12:20884339-20884406	LNCaP	prostate:	n/a	chr12:20884367-20884388 chr12:20884365-20884383
47	CTCF	chr12:20868980-20869130	HAc	cerebellar:	n/a	chr12:20869090-20869108
48	CTCF	chr12:20868960-20869110	HMF	breast:	n/a	chr12:20869090-20869108
49	CTCF	chr12:20869060-20869210	GM06990	blood:	n/a	chr12:20869090-20869108
50	CTCF	chr12:20869020-20869170	GM12871	blood:	n/a	chr12:20869090-20869108

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:20848285-20848335	RPTEC	kidney:	n/a
2	chr12:20848821-20848871	AG04449	skin:	fetal
3	chr12:20848285-20848335	RPTEC	kidney:	n/a
4	chr12:20848821-20848871	AG04449	skin:	fetal
5	chr12:20883886-20883936	MCF10A-Er-Src	breast:	n/a
6	chr12:20847154-20847204	Hela-S3	cervix:	n/a
7	chr12:20848285-20848335	HEEpiC	esophagus:	n/a
8	chr12:20848821-20848871	NHBE	bronchial:	n/a
9	chr12:20847154-20847204	HL-60	blood:	n/a
10	chr12:20847154-20847204	HEK293	kidney:	embryo
11	chr12:20883886-20883936	HAEpiC	amniotic membrane:	n/a
12	chr12:20848285-20848335	SKMC	muscle:	n/a
13	chr12:20847154-20847204	SK-N-SH	brain:	n/a
14	chr12:20848821-20848871	A549	lung:	n/a
15	chr12:20848285-20848335	NHDF-neo	bronchial:	n/a
16	chr12:20883886-20883936	AG09309	skin:	n/a
17	chr12:20848285-20848335	HepG2	liver:	n/a
18	chr12:20848821-20848871	CMK	blood:	n/a
19	chr12:20847154-20847204	HCM	heart:	n/a
20	chr12:20883886-20883936	AG04450	lung:	fetal
21	chr12:20883886-20883936	NHBE	bronchial:	n/a
22	chr12:20848473-20848523	HUVEC	blood vessel:	n/a
23	chr12:20847154-20847204	HCT-116	colon:	n/a
24	chr12:20847154-20847204	AG04449	skin:	fetal
25	chr12:20848285-20848335	ProgFib	skin:	n/a
26	chr12:20883886-20883936	HCF	heart:	n/a
27	chr12:20847154-20847204	ovcar-3	ovarian:	n/a
28	chr12:20883886-20883936	HPAEpiC	pulmonary alveolar:	n/a
29	chr12:20848821-20848871	HMEC	breast:	n/a
30	chr12:20848473-20848523	NB4	blood:	n/a
31	chr12:20848821-20848871	AG10803	skin:	n/a
32	chr12:20848285-20848335	H1-hESC	embryonic stem cell:	embryo
33	chr12:20848473-20848523	NH-A	brain:	n/a
34	chr12:20848285-20848335	AG04450	lung:	fetal
35	chr12:20848821-20848871	HAEpiC	amniotic membrane:	n/a
36	chr12:20848821-20848871	LNCaP	prostate:	n/a
37	chr12:20883886-20883936	A549	lung:	n/a
38	chr12:20848821-20848871	AG09319	gingival:	n/a
39	chr12:20847154-20847204	HCPEpiC	choroid plexus:	n/a
40	chr12:20848285-20848335	BE2_C	brain:	n/a
41	chr12:20848473-20848523	HRE	kidney:	n/a
42	chr12:20883886-20883936	Caco-2	colon:	n/a
43	chr12:20883886-20883936	AoSMC	blood vessel:	n/a
44	chr12:20848473-20848523	NHDF-neo	bronchial:	n/a
45	chr12:20848285-20848335	HL-60	blood:	n/a
46	chr12:20848821-20848871	SKMC	muscle:	n/a
47	chr12:20847154-20847204	NHBE	bronchial:	n/a
48	chr12:20848285-20848335	SK-N-SH_RA	brain:	n/a
49	chr12:20848473-20848523	HPAEpiC	pulmonary alveolar:	n/a
50	chr12:20848473-20848523	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:20886731..20889299-chr12:20891417..20893433,2	K562	blood:
2	chr12:20886731..20889299-chr12:20891417..20893433,2	K562	blood:
3	chr12:20856502..20859066-chr12:20865440..20867058,2	MCF-7	breast:
4	chr12:20856502..20859066-chr12:20865440..20867058,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLCO1C1-1	chr12:20849765-20850430	NONHSAT027233
2	lnc-SLCO1C1-1	chr12:20848289-20848546	NONHSAT027231
3	lnc-SLCO1C1-1	chr12:20848670-20848741	NONHSAT027233
4	lnc-SLCO1C1-1	chr12:20848670-20848741	NONHSAT027231
5	lnc-SLCO1C1-1	chr12:20849683-20849909	NONHSAT027231
6	lnc-SLCO1C1-1	chr12:20852486-20853173	NONHSAT027232
7	lnc-SLCO1C1-1	chr12:20848505-20848546	NONHSAT027233
8	lnc-SLCO1C1-1	chr12:20848670-20848741	NONHSAT027232
9	lnc-SLCO1C1-1	chr12:20848495-20848546	NONHSAT027232

Variant related genes	Relation type
SLCO1C1	TF binding region
SLCO1C1	CpG island

Extended variants
information (count: 1678 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1678 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12578492	chr12:20842041-20842042	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs368122218	chr12:20842075-20842076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs137927950	chr12:20842088-20842089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs372638622	chr12:20842098-20842099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs77107216	chr12:20842099-20842100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112648398	chr12:20842100-20842101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs60244226	chr12:20842101-20842102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78319890	chr12:20842103-20842104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573826159	chr12:20842120-20842121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs59198710	chr12:20842125-20842126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs58106025	chr12:20842127-20842128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs397702727	chr12:20842129-20842130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536231195	chr12:20842156-20842157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111457345	chr12:20842157-20842158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs572302107	chr12:20842202-20842203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540921394	chr12:20842243-20842244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182238564	chr12:20842244-20842245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370063817	chr12:20842274-20842275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs78971988	chr12:20842323-20842324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148315091	chr12:20842341-20842342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543662218	chr12:20842361-20842362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563347949	chr12:20842362-20842363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529031110	chr12:20842367-20842368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149167148	chr12:20842465-20842466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143310927	chr12:20842479-20842480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs151299118	chr12:20842480-20842481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569602255	chr12:20842496-20842497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571933401	chr12:20842530-20842531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11324454	chr12:20842542-20842543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148379085	chr12:20842547-20842548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544023161	chr12:20842556-20842557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs111998092	chr12:20842561-20842562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs551182582	chr12:20842568-20842569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs73240408	chr12:20842596-20842597	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs529001299	chr12:20842640-20842641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs80061976	chr12:20842661-20842662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200003937	chr12:20842671-20842672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573114579	chr12:20842710-20842711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12819256	chr12:20842731-20842732	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs559395331	chr12:20842762-20842763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs7310399	chr12:20842858-20842859	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs73240410	chr12:20842905-20842906	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs543625202	chr12:20842918-20842919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563512078	chr12:20842927-20842928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192502027	chr12:20842986-20842987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs73240412	chr12:20842994-20842995	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs143386929	chr12:20843087-20843088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs145767693	chr12:20843088-20843089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs116163945	chr12:20843191-20843192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184535882	chr12:20843213-20843214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
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
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
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	16397240	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21364760	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:136 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:20834200-20842200	Weak transcription	Ovary	ovary
2	chr12:20834200-20846600	Weak transcription	Fetal Stomach	stomach
3	chr12:20838800-20849800	Weak transcription	Hela-S3	cervix
4	chr12:20846600-20847200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr12:20846600-20847400	Enhancers	Fetal Stomach	stomach
6	chr12:20846800-20847000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr12:20846800-20848000	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr12:20846800-20848200	Enhancers	Adipose Nuclei	Adipose
9	chr12:20847000-20848200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr12:20847000-20848400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr12:20847000-20849400	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr12:20847200-20847600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr12:20847200-20848800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr12:20847400-20848400	Weak transcription	Fetal Stomach	stomach
15	chr12:20847600-20849400	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr12:20847800-20848000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr12:20847800-20848400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr12:20847800-20849400	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr12:20847800-20849800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr12:20847800-20850000	Active TSS	Brain Anterior Caudate	brain
21	chr12:20848000-20848200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr12:20848000-20848200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
23	chr12:20848000-20848200	Active TSS	Fetal Lung	lung
24	chr12:20848000-20848400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr12:20848000-20848600	Enhancers	H9 Cell Line	embryonic stem cell
26	chr12:20848000-20848600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr12:20848000-20848600	Active TSS	Right Atrium	heart
28	chr12:20848000-20848800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr12:20848000-20849000	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr12:20848000-20849200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr12:20848000-20849800	Active TSS	Brain Hippocampus Middle	brain
32	chr12:20848200-20848400	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr12:20848200-20848400	Flanking Active TSS	Fetal Lung	lung
34	chr12:20848200-20848600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr12:20848200-20848600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr12:20848200-20848600	Flanking Active TSS	Adipose Nuclei	Adipose
37	chr12:20848200-20848800	Enhancers	H1 Cell Line	embryonic stem cell
38	chr12:20848200-20848800	Enhancers	NHDF-Ad	bronchial
39	chr12:20848200-20849600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr12:20848400-20848600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
41	chr12:20848400-20848800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr12:20848400-20848800	Active TSS	Brain Cingulate Gyrus	brain
43	chr12:20848400-20848800	Flanking Active TSS	Fetal Stomach	stomach
44	chr12:20848400-20849000	Active TSS	Brain Inferior Temporal Lobe	brain
45	chr12:20848400-20849400	Active TSS	Brain Substantia Nigra	brain
46	chr12:20848400-20849400	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr12:20848400-20849400	Weak transcription	Fetal Lung	lung
48	chr12:20848400-20849800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
49	chr12:20848400-20849800	Enhancers	Fetal Muscle Leg	muscle
50	chr12:20848400-20851800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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