Variant report

Variant	nsv558105
Chromosome Location	chr12:31900550-31912588
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:865)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:865 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:31901939-31902594	K562	blood:	n/a	n/a
2	ARID3A	chr12:31901910-31902691	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:31909974-31910231	HepG2	liver:	n/a	n/a
4	ATF1	chr12:31910164-31910364	K562	blood:	n/a	n/a
5	ATF1	chr12:31902088-31902581	K562	blood:	n/a	n/a
6	ATF2	chr12:31902028-31902526	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr12:31901758-31902687	GM12878	blood:	n/a	n/a
8	ATF2	chr12:31901982-31902503	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr12:31901708-31902645	GM12878	blood:	n/a	n/a
10	ATF3	chr12:31901829-31902705	HCT-116	colon:	n/a	n/a
11	ATF3	chr12:31901886-31902752	A549	lung:	n/a	n/a
12	ATF3	chr12:31901890-31902594	K562	blood:	n/a	n/a
13	ATF3	chr12:31902095-31902409	HepG2	liver:	n/a	n/a
14	ATF3	chr12:31901867-31902659	HCT-116	colon:	n/a	n/a
15	ATF3	chr12:31901857-31902688	A549	lung:	n/a	n/a
16	ATF3	chr12:31909916-31910330	K562	blood:	n/a	n/a
17	ATF3	chr12:31902136-31902441	K562	blood:	n/a	n/a
18	BACH1	chr12:31901909-31902527	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr12:31902009-31902464	K562	blood:	n/a	n/a
20	BATF	chr12:31901977-31902530	GM12878	blood:	n/a	chr12:31902262-31902273
21	BATF	chr12:31911249-31911568	GM12878	blood:	n/a	chr12:31911426-31911437 chr12:31911370-31911381
22	BATF	chr12:31901846-31902653	GM12878	blood:	n/a	chr12:31902262-31902273
23	BCL11A	chr12:31902132-31902376	H1-hESC	embryonic stem cell:	n/a	n/a
24	BCL11A	chr12:31902028-31902625	GM12878	blood:	n/a	n/a
25	BCL11A	chr12:31901905-31902669	GM12878	blood:	n/a	n/a
26	BCL3	chr12:31901804-31902807	A549	lung:	n/a	n/a
27	BCL3	chr12:31901863-31902625	GM12878	blood:	n/a	n/a
28	BCL3	chr12:31901887-31902683	A549	lung:	n/a	n/a
29	BCLAF1	chr12:31903328-31904118	GM12878	blood:	n/a	n/a
30	BCLAF1	chr12:31901863-31902707	GM12878	blood:	n/a	n/a
31	BCLAF1	chr12:31901988-31902644	K562	blood:	n/a	n/a
32	BCLAF1	chr12:31901791-31902693	GM12878	blood:	n/a	n/a
33	BHLHE40	chr12:31902109-31902535	HepG2	liver:	n/a	n/a
34	BHLHE40	chr12:31910013-31910250	GM12878	blood:	n/a	n/a
35	BHLHE40	chr12:31902072-31902616	HepG2	liver:	n/a	n/a
36	BHLHE40	chr12:31901833-31902757	GM12878	blood:	n/a	n/a
37	BHLHE40	chr12:31903115-31903770	GM12878	blood:	n/a	n/a
38	BHLHE40	chr12:31902076-31902628	K562	blood:	n/a	n/a
39	BHLHE40	chr12:31905586-31905714	GM12878	blood:	n/a	n/a
40	BHLHE40	chr12:31909902-31910373	K562	blood:	n/a	n/a
41	BHLHE40	chr12:31902006-31902637	A549	lung:	n/a	n/a
42	BHLHE40	chr12:31902207-31902543	HepG2	liver:	n/a	n/a
43	BRCA1	chr12:31901965-31902603	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr12:31902088-31902529	HepG2	liver:	n/a	n/a
45	BRCA1	chr12:31905289-31905411	GM12878	blood:	n/a	n/a
46	CBX3	chr12:31901830-31902608	K562	blood:	n/a	n/a
47	CBX3	chr12:31901792-31902765	HCT-116	colon:	n/a	n/a
48	CBX3	chr12:31903227-31903855	K562	blood:	n/a	n/a
49	CBX3	chr12:31909939-31910274	K562	blood:	n/a	n/a
50	CBX3	chr12:31901729-31902755	HCT-116	colon:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31902503-31902553	HepG2	liver:	n/a
2	chr12:31902503-31902553	HUVEC	blood vessel:	n/a
3	chr12:31902503-31902553	Caco-2	colon:	n/a
4	chr12:31902503-31902553	ECC-1	luminal epithelium:	n/a
5	chr12:31902503-31902553	NH-A	brain:	n/a
6	chr12:31902503-31902553	AG09309	skin:	n/a
7	chr12:31902503-31902553	HRPEpiC	eye:	n/a
8	chr12:31902503-31902553	CMK	blood:	n/a
9	chr12:31902503-31902553	H1-hESC	embryonic stem cell:	embryo
10	chr12:31902503-31902553	NT2-D1	testis:	n/a
11	chr12:31902503-31902553	HL-60	blood:	n/a
12	chr12:31902503-31902553	Hela-S3	cervix:	n/a
13	chr12:31902503-31902553	NHBE	bronchial:	n/a
14	chr12:31902503-31902553	IMR90	lung:	fetal
15	chr12:31902503-31902553	MCF10A-Er-Src	breast:	n/a
16	chr12:31902503-31902553	GM12891	blood:	n/a
17	chr12:31902503-31902553	NHDF-neo	bronchial:	n/a
18	chr12:31902503-31902553	HRE	kidney:	n/a
19	chr12:31902503-31902553	HCF	heart:	n/a
20	chr12:31902503-31902553	U87	brain:	n/a
21	chr12:31902503-31902553	GM12892	blood:	n/a
22	chr12:31902503-31902553	BE2_C	brain:	n/a
23	chr12:31902503-31902553	HCPEpiC	choroid plexus:	n/a
24	chr12:31902503-31902553	PrEC	prostate:	n/a
25	chr12:31902503-31902553	HCT-116	colon:	n/a
26	chr12:31902503-31902553	HIPEpiC	eye:	n/a
27	chr12:31902503-31902553	ProgFib	skin:	n/a
28	chr12:31902503-31902553	Jurkat	blood:	n/a
29	chr12:31902503-31902553	K562	blood:	n/a
30	chr12:31902503-31902553	HPAEpiC	pulmonary alveolar:	n/a
31	chr12:31902503-31902553	SKMC	muscle:	n/a
32	chr12:31902503-31902553	BJ	skin:	n/a
33	chr12:31902503-31902553	AG10803	skin:	n/a
34	chr12:31902503-31902553	HRCEpiC	kidney:	n/a
35	chr12:31902503-31902553	HNPCEpiC	eye:	n/a
36	chr12:31902503-31902553	NB4	blood:	n/a
37	chr12:31902503-31902553	PANC-1	pancreas:	n/a
38	chr12:31902503-31902553	MCF-7	breast:	n/a
39	chr12:31902503-31902553	ovcar-3	ovarian:	n/a
40	chr12:31902503-31902553	PFSK-1	brain:	n/a
41	chr12:31902503-31902553	LNCaP	prostate:	n/a
42	chr12:31902503-31902553	SK-N-MC	brain:	n/a
43	chr12:31902503-31902553	HEK293	kidney:	embryo
44	chr12:31902503-31902553	HAEpiC	amniotic membrane:	n/a
45	chr12:31902503-31902553	HEEpiC	esophagus:	n/a
46	chr12:31902503-31902553	HMEC	breast:	n/a
47	chr12:31902503-31902553	SK-N-SH	brain:	n/a
48	chr12:31902503-31902553	Hepatocyte	liver:	n/a
49	chr12:31902503-31902553	GM06990	blood:	n/a
50	chr12:31902503-31902553	GM12878	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:31902284..31904041-chr12:31909797..31911614,2	K562	blood:
2	chr12:31902284..31904041-chr12:31909797..31911614,2	K562	blood:
3	chr12:31901857..31902801-chr12:31926002..31926958,3	MCF-7	breast:
4	chr12:31880350..31888706-chr12:31898122..31903847,15	K562	blood:
5	chr12:31906089..31908319-chr12:31910376..31912978,2	K562	blood:
6	chr12:31867508..31869786-chr12:31900848..31903323,2	K562	blood:
7	chr12:31866804..31870237-chr12:31900678..31903673,4	K562	blood:
8	chr12:31897495..31899611-chr12:31901750..31904156,2	MCF-7	breast:
9	chr12:31880356..31882113-chr12:31908651..31911633,2	K562	blood:
10	chr12:31902147..31904881-chr12:32110992..32113730,2	MCF-7	breast:
11	chr12:31880235..31884620-chr12:31906466..31910642,5	K562	blood:
12	chr12:31883178..31885919-chr12:31902028..31904052,3	K562	blood:
13	chr12:31901665..31904041-chr12:31908599..31911297,2	K562	blood:
14	chr12:31901665..31904041-chr12:31908599..31911297,2	K562	blood:
15	chr12:31884351..31886609-chr12:31902358..31904418,2	MCF-7	breast:
16	chr12:31900170..31902250-chr12:31904037..31906770,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-H3F3C-1	chr12:31903114-31904287	XLOC_010043
2	lnc-AMN1-2	chr12:31900809-31901031	NONHSAT027573
3	lnc-H3F3C-1	chr12:31906082-31906270	XLOC_010043

No data

Variant related genes	Relation type
ENSG00000223722	TF binding region
ENSG00000256843	TF binding region
ENSG00000223722	CpG island
ENSG00000256843	CpG island
ENSG00000174718	chromatin interactions
ENSG00000223722	chromatin interactions
ENSG00000256843	chromatin interactions
ENSG00000151743	chromatin interactions
MEOX2	miRNA target sites

Extended variants
information (count: 499 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:499 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11829645	chr12:31900550-31900551	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556885908	chr12:31900700-31900701	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs12318379	chr12:31900750-31900751	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs537817931	chr12:31900756-31900757	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs557752986	chr12:31900765-31900766	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs190337813	chr12:31900789-31900790	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs149063208	chr12:31900798-31900799	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs183008820	chr12:31900818-31900819	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs573748572	chr12:31900839-31900840	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs188245332	chr12:31900840-31900841	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs76002024	chr12:31900843-31900844	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs11051555	chr12:31900855-31900856	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs147080636	chr12:31900874-31900875	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs138478333	chr12:31900878-31900879	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs527785750	chr12:31900887-31900888	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs142596461	chr12:31900914-31900915	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs561569885	chr12:31900938-31900939	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs546363026	chr12:31900968-31900969	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs530215721	chr12:31901018-31901019	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs112793460	chr12:31901021-31901022	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs376328571	chr12:31901028-31901029	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs570383708	chr12:31901054-31901055	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs12302735	chr12:31901091-31901092	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs148297440	chr12:31901194-31901195	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs528716124	chr12:31901219-31901220	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs12316208	chr12:31901236-31901237	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs376388667	chr12:31901240-31901241	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs573809193	chr12:31901241-31901242	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs536066837	chr12:31901285-31901286	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs75818799	chr12:31901309-31901310	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs12367895	chr12:31901312-31901313	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs12302797	chr12:31901327-31901328	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs192463134	chr12:31901328-31901329	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs374069587	chr12:31901330-31901331	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs572339796	chr12:31901341-31901342	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs147694602	chr12:31901392-31901393	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs541547780	chr12:31901399-31901400	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs561202281	chr12:31901403-31901404	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs116161547	chr12:31901409-31901410	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs79650002	chr12:31901472-31901473	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs76229706	chr12:31901474-31901475	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs147731728	chr12:31901506-31901507	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs184378694	chr12:31901524-31901525	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs532903468	chr12:31901525-31901526	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs536983640	chr12:31901559-31901560	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs552895483	chr12:31901560-31901561	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs112080582	chr12:31901630-31901631	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs7955847	chr12:31901637-31901638	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs547343295	chr12:31901694-31901695	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs567266839	chr12:31901709-31901710	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	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
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	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
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
microdeletion syndrome	16199537	CNVD
Chordoma	18071362	CNVD
Cancer	20164920	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:417 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31889400-31905800	Enhancers	Primary B cells from peripheral blood	blood
2	chr12:31893600-31905800	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr12:31894400-31903400	Weak transcription	Spleen	Spleen
4	chr12:31895800-31902000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr12:31896200-31903600	Weak transcription	Fetal Kidney	kidney
6	chr12:31896200-31903600	Weak transcription	Small Intestine	intestine
7	chr12:31896400-31902000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr12:31897600-31902400	Enhancers	Hela-S3	cervix
9	chr12:31898000-31900800	Weak transcription	Colonic Mucosa	Colon
10	chr12:31898800-31900600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr12:31898800-31900800	Enhancers	Primary hematopoietic stem cells	blood
12	chr12:31899000-31900800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr12:31899000-31901000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr12:31899000-31901000	Flanking Active TSS	GM12878-XiMat	blood
15	chr12:31899200-31900600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr12:31899200-31900600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr12:31899200-31900600	Enhancers	HUVEC	blood vessel
18	chr12:31899400-31900600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr12:31899400-31900600	Enhancers	HMEC	breast
20	chr12:31899400-31900600	Enhancers	Osteobl	bone
21	chr12:31899400-31903600	Weak transcription	Lung	lung
22	chr12:31899600-31900600	Enhancers	Placenta	Placenta
23	chr12:31899600-31901000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr12:31899600-31901200	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr12:31899600-31905200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr12:31899800-31902000	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr12:31900000-31900800	Weak transcription	K562	blood
28	chr12:31900000-31901800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr12:31900000-31901800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr12:31900000-31901800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr12:31900000-31901800	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr12:31900000-31901800	Weak transcription	Dnd41	blood
33	chr12:31900000-31902000	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr12:31900000-31902000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr12:31900000-31902000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr12:31900000-31902000	Weak transcription	Liver	Liver
37	chr12:31900000-31902000	Weak transcription	HSMM	muscle
38	chr12:31900000-31902000	Weak transcription	NHLF	lung
39	chr12:31900000-31902200	Weak transcription	Thymus	Thymus
40	chr12:31900000-31903200	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr12:31900000-31903400	Weak transcription	Placenta Amnion	Placenta Amnion
42	chr12:31900000-31903600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr12:31900000-31905200	Weak transcription	Primary T cells from cord blood	blood
44	chr12:31900000-31905800	Enhancers	Primary B cells from cord blood	blood
45	chr12:31900000-31906400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
46	chr12:31900200-31900600	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr12:31900200-31900800	Enhancers	A549	lung
48	chr12:31900200-31901000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr12:31900200-31901200	Enhancers	Muscle Satellite Cultured Cells	--
50	chr12:31900200-31901200	Weak transcription	NHEK	skin

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