Variant report

Variant	esv3448120
Chromosome Location	chr12:120657469-120661667
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:103)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr12:120661593-120661614	K562	blood:	n/a	n/a
2	CHD2	chr12:120659026-120659120	HepG2	liver:	n/a	n/a
3	CTCF	chr12:120661309-120661380	Lung_OC	lung:	n/a	n/a
4	CTCF	chr12:120661240-120661390	HEK293	kidney:	n/a	n/a
5	ELF1	chr12:120659613-120659855	K562	blood:	n/a	chr12:120659740-120659753
6	EP300	chr12:120658909-120658952	HepG2	liver:	n/a	n/a
7	FOS	chr12:120661657-120661864	MCF10A-Er-Src	breast:	n/a	chr12:120661809-120661817
8	FOXA2	chr12:120658615-120658873	HepG2	liver:	n/a	n/a
9	HMGN3	chr12:120657422-120657599	K562	blood:	n/a	n/a
10	MAX	chr12:120658735-120659176	HepG2	liver:	n/a	chr12:120658752-120658761
11	MAX	chr12:120658475-120659359	HepG2	liver:	n/a	chr12:120658696-120658706 chr12:120658752-120658761
12	MYC	chr12:120659790-120659880	GM12878	blood:	n/a	n/a
13	MYC	chr12:120658808-120659226	HepG2	liver:	n/a	n/a
14	POLR2A	chr12:120659362-120659465	MCF-7	breast:	n/a	n/a
15	POLR2A	chr12:120661119-120661966	U87	brain:	n/a	n/a
16	POLR2A	chr12:120659797-120660249	K562	blood:	n/a	n/a
17	POLR2A	chr12:120659400-120659601	A549	lung:	n/a	n/a
18	POLR2A	chr12:120660102-120660317	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr12:120658524-120658560	HUVEC	blood vessel:	n/a	n/a
20	POLR2A	chr12:120657761-120658097	ECC-1	luminal epithelium:	n/a	n/a
21	POLR2A	chr12:120659915-120660437	U87	brain:	n/a	n/a
22	POLR2A	chr12:120658327-120658333	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr12:120660177-120660303	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr12:120659170-120659444	HepG2	liver:	n/a	n/a
25	POLR2A	chr12:120658370-120658917	HUVEC	blood vessel:	n/a	n/a
26	POLR2A	chr12:120659497-120659570	MCF-7	breast:	n/a	n/a
27	POLR2A	chr12:120657609-120657808	K562	blood:	n/a	n/a
28	POLR2A	chr12:120656371-120661011	PANC-1	pancreas:	n/a	n/a
29	POLR2A	chr12:120659095-120659608	U87	brain:	n/a	n/a
30	POLR2A	chr12:120660002-120660006	K562	blood:	n/a	n/a
31	POLR2A	chr12:120659853-120659887	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr12:120658815-120659902	K562	blood:	n/a	n/a
33	POLR2A	chr12:120658952-120659064	K562	blood:	n/a	n/a
34	POLR2A	chr12:120658910-120659734	A549	lung:	n/a	n/a
35	POLR2A	chr12:120659391-120659396	K562	blood:	n/a	n/a
36	POLR2A	chr12:120659445-120659977	K562	blood:	n/a	n/a
37	POLR2A	chr12:120659393-120659402	K562	blood:	n/a	n/a
38	POLR2A	chr12:120659989-120660815	K562	blood:	n/a	n/a
39	POLR2A	chr12:120661113-120662097	U87	brain:	n/a	n/a
40	POLR2A	chr12:120661126-120671187	PANC-1	pancreas:	n/a	n/a
41	POLR2A	chr12:120660011-120660380	A549	lung:	n/a	n/a
42	POLR2A	chr12:120660481-120661004	PANC-1	pancreas:	n/a	n/a
43	POLR2A	chr12:120660564-120660581	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr12:120657496-120657872	Hela-S3	cervix:	n/a	n/a
45	POLR2A	chr12:120661440-120664328	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr12:120658573-120658773	HepG2	liver:	n/a	n/a
47	POLR2A	chr12:120656794-120657914	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr12:120660080-120660348	A549	lung:	n/a	n/a
49	POLR2A	chr12:120658585-120658811	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr12:120657537-120657749	U87	brain:	n/a	n/a

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:120656223..120689871-chr12:120720394..120738112,311	MCF-7	breast:
2	chr12:120657004..120683911-chr12:120723753..120737731,232	K562	blood:
3	chr12:120642171..120684465-chr12:120719749..120734210,267	K562	blood:
4	chr12:120657996..120659579-chr12:120711658..120714031,2	MCF-7	breast:
5	chr12:120637654..120639331-chr12:120657599..120660175,2	K562	blood:
6	chr12:120628211..120641965-chr12:120660551..120674110,39	K562	blood:

No data

Variant related genes	Relation type
PXN	TF binding region
ENSG00000202538	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000123009	chromatin interactions
ENSG00000089154	chromatin interactions
ENSG00000089157	chromatin interactions
ENSG00000255857	chromatin interactions

Extended variants
information (count: 186 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:186 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537180407	chr12:120657478-120657479	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs530896338	chr12:120657505-120657506	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs558321525	chr12:120657512-120657513	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs79352889	chr12:120657544-120657545	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs540674786	chr12:120657709-120657710	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs370039679	chr12:120657710-120657711	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs528680075	chr12:120657713-120657714	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs376688346	chr12:120657742-120657743	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs77876183	chr12:120657778-120657779	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs562421457	chr12:120657782-120657783	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs562362707	chr12:120657803-120657804	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs371342861	chr12:120657816-120657817	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs543892515	chr12:120657817-120657818	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs202247083	chr12:120657823-120657824	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs77248196	chr12:120657841-120657842	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs367895827	chr12:120657850-120657851	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs56758243	chr12:120657853-120657854	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs189545173	chr12:120657863-120657864	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs564686438	chr12:120657903-120657904	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs376471619	chr12:120657925-120657926	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs149982671	chr12:120657933-120657934	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs547432483	chr12:120657952-120657953	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs566969800	chr12:120657953-120657954	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs574603958	chr12:120657962-120657963	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs536023544	chr12:120657965-120657966	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs184071774	chr12:120657970-120657971	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs569559066	chr12:120658015-120658016	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs188628777	chr12:120658025-120658026	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs369039159	chr12:120658107-120658108	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs558186520	chr12:120658120-120658121	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs145128528	chr12:120658161-120658162	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs534048143	chr12:120658166-120658167	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs554210906	chr12:120658258-120658259	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs573783144	chr12:120658267-120658268	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs542399700	chr12:120658285-120658286	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs562482853	chr12:120658294-120658295	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs575929042	chr12:120658314-120658315	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs372988537	chr12:120658330-120658331	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs73415003	chr12:120658358-120658359	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs564739822	chr12:120658359-120658360	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs527247588	chr12:120658372-120658373	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs147811439	chr12:120658445-120658446	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs561020728	chr12:120658491-120658492	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs541534468	chr12:120658527-120658528	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs372541679	chr12:120658550-120658551	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs141237298	chr12:120658576-120658577	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs146967433	chr12:120658644-120658645	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs543987902	chr12:120658645-120658646	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs552068588	chr12:120658663-120658664	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs114323614	chr12:120658697-120658698	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Autism	20841430	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:257 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:120640200-120661800	Weak transcription	GM12878-XiMat	blood
2	chr12:120640200-120662400	Weak transcription	Fetal Brain Male	brain
3	chr12:120643800-120661800	Strong transcription	Fetal Muscle Leg	muscle
4	chr12:120644000-120660400	Strong transcription	Fetal Intestine Small	intestine
5	chr12:120644000-120662600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr12:120644800-120661400	Strong transcription	Fetal Intestine Large	intestine
7	chr12:120646400-120662400	Weak transcription	Right Atrium	heart
8	chr12:120647000-120661400	Strong transcription	Duodenum Mucosa	Duodenum
9	chr12:120647200-120661400	Strong transcription	Fetal Muscle Trunk	muscle
10	chr12:120647400-120661600	Strong transcription	Muscle Satellite Cultured Cells	--
11	chr12:120647600-120659000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr12:120647600-120659200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr12:120647600-120660000	Strong transcription	Stomach Smooth Muscle	stomach
14	chr12:120647600-120661400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr12:120647600-120661400	Strong transcription	Pancreas	Pancrea
16	chr12:120647600-120661800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr12:120647600-120661800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr12:120647600-120661800	Strong transcription	Skeletal Muscle Female	skeletal muscle
19	chr12:120647600-120662000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr12:120647600-120662000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr12:120647600-120662000	Strong transcription	Adipose Nuclei	Adipose
22	chr12:120647600-120662600	Strong transcription	HUES6 Cell Line	embryonic stem cell
23	chr12:120647600-120662600	Strong transcription	Primary monocytes fromperipheralblood	blood
24	chr12:120647600-120662600	Strong transcription	Primary T helper cells fromperipheralblood	blood
25	chr12:120647600-120662600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr12:120647800-120660800	Strong transcription	HUVEC	blood vessel
27	chr12:120647800-120661600	Strong transcription	Placenta Amnion	Placenta Amnion
28	chr12:120647800-120661600	Strong transcription	Skeletal Muscle Male	skeletal muscle
29	chr12:120647800-120661800	Strong transcription	Primary T cells fromperipheralblood	blood
30	chr12:120647800-120662200	Strong transcription	Monocytes-CD14+_RO01746	blood
31	chr12:120648000-120662200	Strong transcription	Primary T helper cells PMA-I stimulated	--
32	chr12:120648000-120662800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr12:120648000-120662800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr12:120648200-120662200	Strong transcription	Fetal Stomach	stomach
35	chr12:120649600-120661800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr12:120649600-120661800	Weak transcription	Fetal Heart	heart
37	chr12:120649800-120661600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
38	chr12:120650000-120661400	Strong transcription	Colonic Mucosa	Colon
39	chr12:120650200-120661400	Strong transcription	Rectal Mucosa Donor 29	rectum
40	chr12:120650600-120661400	Strong transcription	NHEK	skin
41	chr12:120650800-120659000	Weak transcription	Primary B cells from cord blood	blood
42	chr12:120651600-120659600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr12:120651800-120658400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr12:120651800-120659200	Weak transcription	Primary hematopoietic stem cells	blood
45	chr12:120651800-120661400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr12:120652600-120658400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr12:120652800-120658400	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr12:120653400-120658800	Weak transcription	Small Intestine	intestine
49	chr12:120654000-120658000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr12:120654000-120661400	Strong transcription	Placenta	Placenta

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