Variant report

Variant	nsv898772
Chromosome Location	chr12:10622047-10722585
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:701)
CpG islands
(count:366)
Chromatin interactive
region (count:17)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:701 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:10653777-10653877	K562	blood:	n/a	n/a
2	ATF2	chr12:10709784-10711202	GM12878	blood:	n/a	n/a
3	ATF2	chr12:10695883-10696624	GM12878	blood:	n/a	n/a
4	ATF2	chr12:10693081-10694102	GM12878	blood:	n/a	n/a
5	ATF2	chr12:10693152-10694036	GM12878	blood:	n/a	n/a
6	ATF2	chr12:10695894-10696491	GM12878	blood:	n/a	n/a
7	ATF2	chr12:10710819-10711219	GM12878	blood:	n/a	n/a
8	ATF2	chr12:10709941-10710817	GM12878	blood:	n/a	n/a
9	BATF	chr12:10710332-10710715	GM12878	blood:	n/a	n/a
10	BATF	chr12:10693317-10693939	GM12878	blood:	n/a	chr12:10693650-10693661
11	BATF	chr12:10641906-10642182	GM12878	blood:	n/a	chr12:10642014-10642025
12	BATF	chr12:10696061-10696446	GM12878	blood:	n/a	n/a
13	BATF	chr12:10693300-10693868	GM12878	blood:	n/a	chr12:10693650-10693661
14	BATF	chr12:10710979-10711269	GM12878	blood:	n/a	chr12:10711145-10711156
15	BATF	chr12:10696036-10696487	GM12878	blood:	n/a	n/a
16	BATF	chr12:10641882-10642185	GM12878	blood:	n/a	chr12:10642014-10642025
17	BCL11A	chr12:10671811-10671985	GM12878	blood:	n/a	n/a
18	BCL11A	chr12:10696076-10696426	GM12878	blood:	n/a	n/a
19	BCL11A	chr12:10693310-10693858	GM12878	blood:	n/a	n/a
20	BCL11A	chr12:10693354-10693625	GM12878	blood:	n/a	n/a
21	BCL11A	chr12:10710317-10710684	GM12878	blood:	n/a	n/a
22	BCL11A	chr12:10696199-10696390	GM12878	blood:	n/a	n/a
23	BCL3	chr12:10693210-10693959	GM12878	blood:	n/a	n/a
24	BCL3	chr12:10693360-10693849	GM12878	blood:	n/a	n/a
25	BCL3	chr12:10696031-10696586	GM12878	blood:	n/a	n/a
26	BCL3	chr12:10710259-10710760	GM12878	blood:	n/a	chr12:10710710-10710719
27	BCL3	chr12:10695995-10696628	GM12878	blood:	n/a	n/a
28	BCL3	chr12:10711751-10712163	GM12878	blood:	n/a	chr12:10711876-10711885
29	BCLAF1	chr12:10693217-10694044	GM12878	blood:	n/a	n/a
30	BCLAF1	chr12:10696071-10696445	GM12878	blood:	n/a	n/a
31	BCLAF1	chr12:10707757-10708159	GM12878	blood:	n/a	n/a
32	BCLAF1	chr12:10714764-10715278	GM12878	blood:	n/a	chr12:10715136-10715145
33	BCLAF1	chr12:10693241-10693808	GM12878	blood:	n/a	n/a
34	BCLAF1	chr12:10706665-10707710	GM12878	blood:	n/a	n/a
35	BCLAF1	chr12:10709854-10710814	GM12878	blood:	n/a	chr12:10710710-10710719
36	BHLHE40	chr12:10693305-10693679	GM12878	blood:	n/a	n/a
37	BHLHE40	chr12:10710383-10710761	GM12878	blood:	n/a	n/a
38	BRCA1	chr12:10676248-10676302	GM12878	blood:	n/a	n/a
39	BRCA1	chr12:10710053-10710128	GM12878	blood:	n/a	n/a
40	CEBPB	chr12:10716337-10716441	HepG2	liver:	n/a	n/a
41	CEBPB	chr12:10706586-10708245	GM12878	blood:	n/a	n/a
42	CEBPB	chr12:10695688-10696520	GM12878	blood:	n/a	n/a
43	CEBPB	chr12:10693180-10693997	GM12878	blood:	n/a	n/a
44	CEBPB	chr12:10675319-10675536	HepG2	liver:	n/a	chr12:10675436-10675447
45	CEBPB	chr12:10705717-10706316	GM12878	blood:	n/a	n/a
46	CEBPB	chr12:10709894-10710828	GM12878	blood:	n/a	n/a
47	CEBPB	chr12:10675342-10675509	A549	lung:	n/a	chr12:10675436-10675447
48	CREB1	chr12:10693203-10694090	GM12878	blood:	n/a	n/a
49	CREB1	chr12:10674190-10674624	GM12878	blood:	n/a	n/a
50	CREB1	chr12:10693316-10693819	GM12878	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10704318-10704368	HCM	heart:	n/a
2	chr12:10658281-10658331	HCPEpiC	choroid plexus:	n/a
3	chr12:10704074-10704124	NT2-D1	testis:	n/a
4	chr12:10658281-10658331	HRCEpiC	kidney:	n/a
5	chr12:10658539-10658589	HRPEpiC	eye:	n/a
6	chr12:10658539-10658589	SK-N-MC	brain:	n/a
7	chr12:10704074-10704124	HAEpiC	amniotic membrane:	n/a
8	chr12:10658281-10658331	AG04449	skin:	fetal
9	chr12:10704074-10704124	PFSK-1	brain:	n/a
10	chr12:10704009-10704059	NB4	blood:	n/a
11	chr12:10658539-10658589	GM12892	blood:	n/a
12	chr12:10704318-10704368	AG10803	skin:	n/a
13	chr12:10658539-10658589	NH-A	brain:	n/a
14	chr12:10658281-10658331	HCT-116	colon:	n/a
15	chr12:10658425-10658475	Jurkat	blood:	n/a
16	chr12:10658425-10658475	U87	brain:	n/a
17	chr12:10658539-10658589	AG09319	gingival:	n/a
18	chr12:10704009-10704059	RPTEC	kidney:	n/a
19	chr12:10658425-10658475	AG10803	skin:	n/a
20	chr12:10704009-10704059	HMEC	breast:	n/a
21	chr12:10704074-10704124	T-47D	breast:	n/a
22	chr12:10658425-10658475	NH-A	brain:	n/a
23	chr12:10658539-10658589	PrEC	prostate:	n/a
24	chr12:10658425-10658475	H1-hESC	embryonic stem cell:	embryo
25	chr12:10658425-10658475	Caco-2	colon:	n/a
26	chr12:10704009-10704059	IMR90	lung:	fetal
27	chr12:10658281-10658331	ECC-1	luminal epithelium:	n/a
28	chr12:10704009-10704059	HEEpiC	esophagus:	n/a
29	chr12:10704318-10704368	Hepatocyte	liver:	n/a
30	chr12:10704318-10704368	HRE	kidney:	n/a
31	chr12:10658281-10658331	AG09319	gingival:	n/a
32	chr12:10704074-10704124	HCM	heart:	n/a
33	chr12:10658281-10658331	HPAEpiC	pulmonary alveolar:	n/a
34	chr12:10704009-10704059	HCM	heart:	n/a
35	chr12:10658281-10658331	NHDF-neo	bronchial:	n/a
36	chr12:10704318-10704368	U87	brain:	n/a
37	chr12:10704318-10704368	PrEC	prostate:	n/a
38	chr12:10704074-10704124	PrEC	prostate:	n/a
39	chr12:10658539-10658589	MCF10A-Er-Src	breast:	n/a
40	chr12:10704074-10704124	Caco-2	colon:	n/a
41	chr12:10658281-10658331	PFSK-1	brain:	n/a
42	chr12:10704009-10704059	H1-hESC	embryonic stem cell:	embryo
43	chr12:10704074-10704124	LNCaP	prostate:	n/a
44	chr12:10704009-10704059	GM12891	blood:	n/a
45	chr12:10658425-10658475	NT2-D1	testis:	n/a
46	chr12:10658539-10658589	GM12878	blood:	n/a
47	chr12:10658425-10658475	ECC-1	luminal epithelium:	n/a
48	chr12:10704318-10704368	ovcar-3	ovarian:	n/a
49	chr12:10704074-10704124	SK-N-SH	brain:	n/a
50	chr12:10658539-10658589	PANC-1	pancreas:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:10484283..10485072-chr12:10714510..10715568,4	K562	blood:
2	chr12:10483978..10484906-chr12:10714545..10715159,3	MCF-7	breast:
3	chr12:10722202..10724547-chr12:10764643..10766915,2	K562	blood:
4	chr12:10713530..10716257-chr12:10762530..10764410,2	MCF-7	breast:
5	chr12:10714679..10715464-chr12:10826841..10827362,2	MCF-7	breast:
6	chr12:10714739..10715346-chr12:10902495..10903116,2	K562	blood:
7	chr12:10388060..10389289-chr12:10714524..10715522,5	MCF-7	breast:
8	chr12:10484099..10484956-chr12:10652861..10653779,2	MCF-7	breast:
9	chr12:10693047..10695502-chr12:10698886..10701191,2	K562	blood:
10	chr12:10484044..10484911-chr12:10711156..10712037,3	MCF-7	breast:
11	chr12:10392959..10394973-chr12:10709982..10712933,2	MCF-7	breast:
12	chr12:10693047..10695502-chr12:10698886..10701191,2	K562	blood:
13	chr12:10388138..10389062-chr12:10714617..10715220,3	K562	blood:
14	chr12:10389063..10390009-chr12:10714674..10715483,2	K562	blood:
15	chr12:10305944..10306449-chr12:10714647..10715601,2	MCF-7	breast:
16	chr12:10484385..10484963-chr12:10714626..10715246,2	MCF-7	breast:
17	chr12:10388252..10388816-chr12:10653557..10654233,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF2S3L.1-1	chr12:10709642-10712295	NONHSAT026886
2	lnc-EIF2S3L.1-5	chr12:10717846-10718105	predAs_ge08_STYK1_1
3	lnc-EIF2S3L.1-1	chr12:10706698-10706732	NONHSAT026886
4	lnc-EIF2S3L.1-1	chr12:10705962-10706115	ENSG00000256039
5	lnc-EIF2S3L.1-1	chr12:10705979-10706115	XLOC_009661
6	lnc-EIF2S3L.1-4	chr12:10703809-10704403	NONHSAT026884
7	lnc-EIF2S3L.1-1	chr12:10705975-10706120	NONHSAT026886
8	lnc-EIF2S3L.1-1	chr12:10709935-10710816	XLOC_009661
9	lnc-MAGOHB-2	chr12:10703865-10704134	NONHSAT026885
10	lnc-EIF2S3L.1-1	chr12:10709935-10710648	ENSG00000256039

No data

Variant related genes	Relation type
ENSG00000180574	TF binding region
ENSG00000256039	TF binding region
SLC25A39P2	TF binding region
ENSG00000180574	CpG island
ENSG00000256039	CpG island
SLC25A39P2	CpG island
ENSG00000060140	chromatin interactions
ENSG00000111196	chromatin interactions
ENSG00000256888	chromatin interactions
MAP7	miRNA target sites
RBM12B	miRNA target sites
PHKA1	miRNA target sites
CMTM4	miRNA target sites

Extended variants
information (count: 2358 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2358 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2900421	chr12:10622047-10622048	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs554866579	chr12:10622100-10622101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191200512	chr12:10622117-10622118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs573183921	chr12:10622142-10622143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529055369	chr12:10622156-10622157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs376211886	chr12:10622164-10622165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs77071066	chr12:10622175-10622176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs538094415	chr12:10622183-10622184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs551398017	chr12:10622245-10622246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs571231569	chr12:10622266-10622267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs6488290	chr12:10622275-10622276	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs553567581	chr12:10622285-10622286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs573434212	chr12:10622293-10622294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs368112647	chr12:10622298-10622299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs11614291	chr12:10622315-10622316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146830539	chr12:10622325-10622326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529371785	chr12:10622378-10622379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs371583957	chr12:10622394-10622395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148955564	chr12:10622419-10622420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs180852616	chr12:10622423-10622424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374881335	chr12:10622424-10622425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544477363	chr12:10622461-10622462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564155679	chr12:10622472-10622473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs143687801	chr12:10622474-10622475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549241278	chr12:10622499-10622500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540355699	chr12:10622520-10622521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540650018	chr12:10622523-10622524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369600739	chr12:10622543-10622544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs529125369	chr12:10622561-10622562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187414256	chr12:10622590-10622591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs562653607	chr12:10622624-10622625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531659133	chr12:10622625-10622626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561906803	chr12:10622626-10622627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571294979	chr12:10622643-10622644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533770037	chr12:10622644-10622645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148090954	chr12:10622661-10622662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191826611	chr12:10622674-10622675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536300242	chr12:10622675-10622676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527536360	chr12:10622687-10622688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555704945	chr12:10622803-10622804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547664418	chr12:10622833-10622834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544845814	chr12:10622882-10622883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570656762	chr12:10622972-10622973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10845133	chr12:10622979-10622980	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs12578507	chr12:10622995-10622996	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs140921020	chr12:10623075-10623076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577661381	chr12:10623139-10623140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146912061	chr12:10623146-10623147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549816304	chr12:10623179-10623180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560456510	chr12:10623186-10623187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	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
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:242 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10607600-10625400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:10621200-10622400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
3	chr12:10631200-10631600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
4	chr12:10631400-10631600	ZNF genes & repeats	Thymus	Thymus
5	chr12:10631600-10631800	Enhancers	Thymus	Thymus
6	chr12:10633000-10635600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr12:10633800-10635000	Enhancers	Primary T cells from cord blood	blood
8	chr12:10633800-10635400	Enhancers	Primary T cells fromperipheralblood	blood
9	chr12:10633800-10635400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr12:10634000-10635400	Enhancers	Primary B cells from peripheral blood	blood
11	chr12:10634000-10635400	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr12:10634800-10635400	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr12:10646400-10646600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr12:10646400-10646800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr12:10649800-10651600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
16	chr12:10650200-10650400	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr12:10650200-10651800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr12:10650400-10650800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr12:10650400-10651000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr12:10650600-10652000	Enhancers	Primary T helper naive cells from peripheral blood	blood
21	chr12:10651000-10651800	Enhancers	Primary T killer memory cells from peripheral blood	blood
22	chr12:10651600-10652000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
23	chr12:10651600-10652200	Enhancers	GM12878-XiMat	blood
24	chr12:10651800-10652000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr12:10652000-10652200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr12:10652000-10652400	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
27	chr12:10652000-10652400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
28	chr12:10652400-10656800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr12:10652800-10654200	Enhancers	Hela-S3	cervix
30	chr12:10653800-10654200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr12:10653800-10654200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr12:10655600-10656000	Enhancers	Brain Hippocampus Middle	brain
33	chr12:10656000-10656400	Flanking Active TSS	Brain Hippocampus Middle	brain
34	chr12:10663200-10663400	Bivalent/Poised TSS	Primary T helper memory cells from peripheral blood 1	blood
35	chr12:10663600-10665200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr12:10664400-10664800	Active TSS	Brain Hippocampus Middle	brain
37	chr12:10664600-10665000	Active TSS	Brain Anterior Caudate	brain
38	chr12:10664600-10665200	Enhancers	Brain Substantia Nigra	brain
39	chr12:10664800-10665000	Flanking Active TSS	Brain Hippocampus Middle	brain
40	chr12:10665000-10666200	Enhancers	Brain Hippocampus Middle	brain
41	chr12:10665200-10665600	Enhancers	Hela-S3	cervix
42	chr12:10674000-10674600	Enhancers	GM12878-XiMat	blood
43	chr12:10678000-10680800	Weak transcription	Fetal Intestine Small	intestine
44	chr12:10680200-10681000	Enhancers	Fetal Intestine Large	intestine
45	chr12:10680600-10680800	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr12:10680800-10681200	Active TSS	Duodenum Mucosa	Duodenum
47	chr12:10680800-10681200	Enhancers	Fetal Intestine Small	intestine
48	chr12:10680800-10681200	Active TSS	Rectal Mucosa Donor 29	rectum
49	chr12:10680800-10681200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
50	chr12:10680800-10681200	Enhancers	Sigmoid Colon	Sigmoid Colon

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