Variant report

Variant	nsv559391
Chromosome Location	chr12:74355828-74505531
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:630)
CpG islands
(count:183)
Chromatin interactive
region (count:28)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:74415614-74416259	K562	blood:	n/a	n/a
2	ARID3A	chr12:74416890-74416941	K562	blood:	n/a	n/a
3	ARID3A	chr12:74437204-74437450	K562	blood:	n/a	n/a
4	ATF1	chr12:74505524-74505833	K562	blood:	n/a	n/a
5	ATF1	chr12:74433064-74433212	K562	blood:	n/a	n/a
6	ATF1	chr12:74415634-74416199	K562	blood:	n/a	n/a
7	ATF3	chr12:74415787-74416157	K562	blood:	n/a	n/a
8	ATF3	chr12:74415536-74416125	A549	lung:	n/a	n/a
9	ATF3	chr12:74436987-74437740	A549	lung:	n/a	n/a
10	BACH1	chr12:74437098-74437429	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr12:74436693-74436701	K562	blood:	n/a	n/a
12	BACH1	chr12:74437237-74437436	K562	blood:	n/a	n/a
13	BCL3	chr12:74436864-74437725	A549	lung:	n/a	n/a
14	BHLHE40	chr12:74415667-74416150	K562	blood:	n/a	n/a
15	BHLHE40	chr12:74402950-74402962	K562	blood:	n/a	n/a
16	BRCA1	chr12:74434492-74434514	GM12878	blood:	n/a	n/a
17	BRCA1	chr12:74382302-74382380	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr12:74436882-74437716	HCT-116	colon:	n/a	n/a
19	CBX3	chr12:74415647-74416021	K562	blood:	n/a	n/a
20	CBX3	chr12:74505433-74505896	HCT-116	colon:	n/a	n/a
21	CBX3	chr12:74436945-74437658	HCT-116	colon:	n/a	n/a
22	CBX3	chr12:74415640-74416084	K562	blood:	n/a	n/a
23	CCNT2	chr12:74415757-74416216	K562	blood:	n/a	n/a
24	CEBPB	chr12:74415624-74416265	K562	blood:	n/a	n/a
25	CEBPB	chr12:74398911-74399207	K562	blood:	n/a	n/a
26	CEBPB	chr12:74505523-74505779	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr12:74399081-74399271	A549	lung:	n/a	n/a
28	CEBPB	chr12:74437025-74437712	MCF-7	breast:	n/a	n/a
29	CEBPB	chr12:74415768-74416234	K562	blood:	n/a	n/a
30	CEBPB	chr12:74401087-74401214	A549	lung:	n/a	n/a
31	CEBPB	chr12:74445592-74445973	H1-hESC	embryonic stem cell:	n/a	chr12:74445783-74445794 chr12:74445783-74445794
32	CEBPB	chr12:74403188-74403466	A549	lung:	n/a	chr12:74403356-74403367
33	CEBPB	chr12:74363029-74363312	IMR90	lung:	n/a	chr12:74363150-74363161 chr12:74363150-74363159 chr12:74363150-74363159 chr12:74363150-74363159 chr12:74363215-74363226 chr12:74363125-74363137 chr12:74363150-74363159
34	CEBPB	chr12:74403192-74403458	HepG2	liver:	n/a	chr12:74403356-74403367
35	CEBPB	chr12:74436997-74437695	A549	lung:	n/a	n/a
36	CEBPB	chr12:74456800-74457031	A549	lung:	n/a	chr12:74456926-74456937
37	CEBPB	chr12:74436923-74437728	HCT-116	colon:	n/a	n/a
38	CEBPB	chr12:74456774-74456982	HepG2	liver:	n/a	chr12:74456926-74456937
39	CEBPB	chr12:74415769-74416185	HepG2	liver:	n/a	n/a
40	CEBPB	chr12:74444888-74445088	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr12:74355992-74356257	HepG2	liver:	n/a	chr12:74356100-74356111
42	CEBPB	chr12:74436955-74437818	A549	lung:	n/a	n/a
43	CEBPB	chr12:74415688-74416147	A549	lung:	n/a	n/a
44	CEBPB	chr12:74362993-74363267	A549	lung:	n/a	chr12:74363150-74363161 chr12:74363150-74363159 chr12:74363150-74363159 chr12:74363150-74363159 chr12:74363215-74363226 chr12:74363125-74363137 chr12:74363150-74363159
45	CEBPB	chr12:74356715-74356913	HepG2	liver:	n/a	chr12:74356844-74356855 chr12:74356844-74356857 chr12:74356845-74356856 chr12:74356844-74356857
46	CEBPB	chr12:74400232-74400470	HepG2	liver:	n/a	chr12:74400328-74400339
47	CEBPB	chr12:74415929-74416125	K562	blood:	n/a	n/a
48	CEBPB	chr12:74437013-74437712	MCF-7	breast:	n/a	n/a
49	CEBPB	chr12:74437045-74437671	A549	lung:	n/a	n/a
50	CEBPB	chr12:74398796-74399307	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:74442868-74442918	AG09309	skin:	n/a
2	chr12:74431418-74431468	NB4	blood:	n/a
3	chr12:74431418-74431468	HL-60	blood:	n/a
4	chr12:74444245-74444295	SK-N-SH	brain:	n/a
5	chr12:74444245-74444295	NH-A	brain:	n/a
6	chr12:74442868-74442918	BJ	skin:	n/a
7	chr12:74442868-74442918	HRE	kidney:	n/a
8	chr12:74431418-74431468	HAEpiC	amniotic membrane:	n/a
9	chr12:74431418-74431468	A549	lung:	n/a
10	chr12:74442868-74442918	GM12892	blood:	n/a
11	chr12:74431418-74431468	HRCEpiC	kidney:	n/a
12	chr12:74444245-74444295	MCF-7	breast:	n/a
13	chr12:74431418-74431468	SKMC	muscle:	n/a
14	chr12:74442868-74442918	A549	lung:	n/a
15	chr12:74442868-74442918	HUVEC	blood vessel:	n/a
16	chr12:74444245-74444295	AG09319	gingival:	n/a
17	chr12:74431418-74431468	PANC-1	pancreas:	n/a
18	chr12:74431418-74431468	BJ	skin:	n/a
19	chr12:74444245-74444295	ECC-1	luminal epithelium:	n/a
20	chr12:74442868-74442918	HPAEpiC	pulmonary alveolar:	n/a
21	chr12:74431418-74431468	Jurkat	blood:	n/a
22	chr12:74431418-74431468	RPTEC	kidney:	n/a
23	chr12:74444245-74444295	NB4	blood:	n/a
24	chr12:74442868-74442918	HNPCEpiC	eye:	n/a
25	chr12:74444245-74444295	Hepatocyte	liver:	n/a
26	chr12:74444245-74444295	HCT-116	colon:	n/a
27	chr12:74431418-74431468	AG04449	skin:	fetal
28	chr12:74431418-74431468	SK-N-SH_RA	brain:	n/a
29	chr12:74442868-74442918	Caco-2	colon:	n/a
30	chr12:74431418-74431468	T-47D	breast:	n/a
31	chr12:74431418-74431468	NHBE	bronchial:	n/a
32	chr12:74442868-74442918	ovcar-3	ovarian:	n/a
33	chr12:74442868-74442918	ProgFib	skin:	n/a
34	chr12:74444245-74444295	GM12892	blood:	n/a
35	chr12:74431418-74431468	MCF-7	breast:	n/a
36	chr12:74442868-74442918	GM06990	blood:	n/a
37	chr12:74444245-74444295	RPTEC	kidney:	n/a
38	chr12:74431418-74431468	HEK293	kidney:	embryo
39	chr12:74431418-74431468	CMK	blood:	n/a
40	chr12:74442868-74442918	NT2-D1	testis:	n/a
41	chr12:74442868-74442918	NHBE	bronchial:	n/a
42	chr12:74444245-74444295	BE2_C	brain:	n/a
43	chr12:74431418-74431468	SK-N-MC	brain:	n/a
44	chr12:74444245-74444295	HPAEpiC	pulmonary alveolar:	n/a
45	chr12:74442868-74442918	HL-60	blood:	n/a
46	chr12:74442868-74442918	SK-N-SH_RA	brain:	n/a
47	chr12:74444245-74444295	HRPEpiC	eye:	n/a
48	chr12:74444245-74444295	Hela-S3	cervix:	n/a
49	chr12:74431418-74431468	PrEC	prostate:	n/a
50	chr12:74442868-74442918	NB4	blood:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:74412851..74416125-chr12:74417786..74420927,4	MCF-7	breast:
2	chr12:74489819..74492327-chr12:74494030..74495535,2	K562	blood:
3	chr12:74443201..74445435-chr12:74461454..74463551,2	MCF-7	breast:
4	chr12:74491549..74494531-chr12:74496083..74497929,2	K562	blood:
5	chr12:74439944..74442321-chr12:74443241..74445352,2	MCF-7	breast:
6	chr12:74491549..74494531-chr12:74496083..74497929,2	K562	blood:
7	chr12:74421024..74423356-chr12:74425327..74427373,2	K562	blood:
8	chr12:74417711..74420682-chr12:74422283..74426238,3	K562	blood:
9	chr12:74412851..74416125-chr12:74417786..74420927,4	MCF-7	breast:
10	chr12:74447256..74448968-chr12:74473500..74476491,2	MCF-7	breast:
11	chr12:74421024..74423356-chr12:74425327..74427373,2	K562	blood:
12	chr12:74417711..74420682-chr12:74422283..74426238,3	K562	blood:
13	chr12:74415229..74416317-chr12:74501474..74502787,6	MCF-7	breast:
14	chr12:74406595..74409366-chr12:74411193..74413349,2	MCF-7	breast:
15	chr12:74443201..74445435-chr12:74461454..74463551,2	MCF-7	breast:
16	chr12:74415343..74416036-chr12:74759116..74760027,3	MCF-7	breast:
17	chr12:74415701..74416228-chr12:74504378..74504925,2	MCF-7	breast:
18	chr12:74439944..74442321-chr12:74443241..74445352,2	MCF-7	breast:
19	chr12:74505191..74505755-chr12:74710574..74711440,3	MCF-7	breast:
20	chr12:74489819..74492327-chr12:74494030..74495535,2	K562	blood:
21	chr12:74415312..74416230-chr12:74710631..74711359,2	MCF-7	breast:
22	chr12:74389722..74391980-chr12:74584509..74586133,2	K562	blood:
23	chr12:74415701..74416228-chr12:74504378..74504925,2	MCF-7	breast:
24	chr12:74415229..74416317-chr12:74501474..74502787,6	MCF-7	breast:
25	chr12:74415389..74416204-chr12:74806037..74807059,3	MCF-7	breast:
26	chr12:74505239..74506034-chr12:74759124..74759988,3	MCF-7	breast:
27	chr12:74447256..74448968-chr12:74473500..74476491,2	MCF-7	breast:
28	chr12:74505235..74505774-chr12:74710528..74711393,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATXN7L3B-1	chr12:74439438-74439608	ENSG00000258332
2	lnc-ATXN7L3B-1	chr12:74432866-74433237	ENSG00000258332

No data

Variant related genes	Relation type
ENSG00000258332	TF binding region
ENSG00000264155	TF binding region
ENSG00000258332	CpG island
ENSG00000264155	CpG island
ENSG00000264155	chromatin interactions
ZNF148	miRNA target sites
TRIM2	miRNA target sites

Extended variants
information (count: 1105 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1105 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560257380	chr12:74367020-74367021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532324978	chr12:74367119-74367120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs112632852	chr12:74367143-74367144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs552399464	chr12:74367201-74367202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562551987	chr12:74367264-74367265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs932143	chr12:74367283-74367284	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs184705990	chr12:74367325-74367326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568193057	chr12:74367355-74367356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs560132870	chr12:74367357-74367358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs529087069	chr12:74367414-74367415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534265280	chr12:74367462-74367463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189494349	chr12:74367510-74367511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs185277528	chr12:74367512-74367513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs145210579	chr12:74367519-74367520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs375984314	chr12:74367574-74367575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539754471	chr12:74367595-74367596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs370614747	chr12:74367658-74367659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs17112931	chr12:74367675-74367676	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs191877889	chr12:74367699-74367700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185361666	chr12:74367766-74367767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs554741594	chr12:74367791-74367792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574598205	chr12:74367792-74367793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs540293506	chr12:74367796-74367797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs73172359	chr12:74367834-74367835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs576925298	chr12:74367920-74367921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545818990	chr12:74367996-74367997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558694936	chr12:74371810-74371811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575556282	chr12:74371830-74371831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs544459200	chr12:74371843-74371844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs189353598	chr12:74371852-74371853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs528869331	chr12:74371856-74371857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs577596097	chr12:74371858-74371859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542752285	chr12:74371894-74371895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs559159692	chr12:74371895-74371896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs117263142	chr12:74371922-74371923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs377645481	chr12:74371967-74371968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs111491986	chr12:74371970-74371971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs117744241	chr12:74371971-74371972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573985611	chr12:74371987-74371988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs550884679	chr12:74371992-74371993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs373246891	chr12:74372010-74372011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs542937355	chr12:74372016-74372017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs536231578	chr12:74372030-74372031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs4020079	chr12:74372063-74372064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553468062	chr12:74372064-74372065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566870527	chr12:74372065-74372066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539097634	chr12:74372071-74372072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs558732067	chr12:74372088-74372089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs575396495	chr12:74372105-74372106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs187351437	chr12:74372141-74372142	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
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
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	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
Hodgkin''s lymphoma	18641027	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:74367000-74368000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr12:74367200-74367600	Enhancers	Brain Germinal Matrix	brain
3	chr12:74367600-74368000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr12:74371800-74372200	Enhancers	H1 Cell Line	embryonic stem cell
5	chr12:74390600-74391000	Enhancers	Brain Hippocampus Middle	brain
6	chr12:74404800-74405000	Enhancers	H9 Cell Line	embryonic stem cell
7	chr12:74404800-74405600	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr12:74404800-74406000	Enhancers	H1 Cell Line	embryonic stem cell
9	chr12:74404800-74406000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr12:74405400-74406200	Enhancers	Placenta Amnion	Placenta Amnion
11	chr12:74406200-74408200	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr12:74408200-74408400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr12:74408200-74408600	Enhancers	Placenta Amnion	Placenta Amnion
14	chr12:74408400-74408600	Enhancers	H9 Cell Line	embryonic stem cell
15	chr12:74408600-74413400	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr12:74411000-74411400	Enhancers	Liver	Liver
17	chr12:74411000-74411400	Enhancers	A549	lung
18	chr12:74411400-74415400	Weak transcription	A549	lung
19	chr12:74412000-74413000	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr12:74412000-74413200	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr12:74412200-74413000	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr12:74412400-74413000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr12:74412600-74413000	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr12:74412600-74413000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr12:74415400-74415800	Enhancers	A549	lung
26	chr12:74415600-74416000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr12:74415600-74416000	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr12:74415600-74416000	Enhancers	K562	blood
29	chr12:74415800-74416000	Enhancers	Pancreas	Pancrea
30	chr12:74415800-74416000	Enhancers	Spleen	Spleen
31	chr12:74415800-74416000	Flanking Active TSS	A549	lung
32	chr12:74416000-74416200	Active TSS	A549	lung
33	chr12:74426800-74427600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr12:74431400-74432000	Enhancers	K562	blood
35	chr12:74432000-74433000	Weak transcription	K562	blood
36	chr12:74433000-74433200	Enhancers	K562	blood
37	chr12:74434600-74436200	Enhancers	Placenta	Placenta
38	chr12:74435800-74436200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr12:74435800-74436800	Enhancers	A549	lung
40	chr12:74435800-74437600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr12:74435800-74438000	Enhancers	NHEK	skin
42	chr12:74436000-74438000	Enhancers	HMEC	breast
43	chr12:74436200-74436600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr12:74436600-74436800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr12:74436600-74437800	Enhancers	Muscle Satellite Cultured Cells	--
46	chr12:74436800-74437000	Flanking Active TSS	A549	lung
47	chr12:74436800-74437400	Enhancers	NH-A	brain
48	chr12:74436800-74440200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr12:74437000-74437400	Active TSS	A549	lung
50	chr12:74437200-74437600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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