Variant report

Variant	nsv898773
Chromosome Location	chr12:10660850-10722585
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:531)
CpG islands
(count:183)
Chromatin interactive
region (count:15)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:531 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:10693081-10694102	GM12878	blood:	n/a	n/a
2	ATF2	chr12:10695883-10696624	GM12878	blood:	n/a	n/a
3	ATF2	chr12:10709941-10710817	GM12878	blood:	n/a	n/a
4	ATF2	chr12:10695894-10696491	GM12878	blood:	n/a	n/a
5	ATF2	chr12:10693152-10694036	GM12878	blood:	n/a	n/a
6	ATF2	chr12:10710819-10711219	GM12878	blood:	n/a	n/a
7	ATF2	chr12:10709784-10711202	GM12878	blood:	n/a	n/a
8	BATF	chr12:10693317-10693939	GM12878	blood:	n/a	chr12:10693650-10693661
9	BATF	chr12:10696061-10696446	GM12878	blood:	n/a	n/a
10	BATF	chr12:10696036-10696487	GM12878	blood:	n/a	n/a
11	BATF	chr12:10693300-10693868	GM12878	blood:	n/a	chr12:10693650-10693661
12	BATF	chr12:10710332-10710715	GM12878	blood:	n/a	n/a
13	BATF	chr12:10710979-10711269	GM12878	blood:	n/a	chr12:10711145-10711156
14	BCL11A	chr12:10696199-10696390	GM12878	blood:	n/a	n/a
15	BCL11A	chr12:10693354-10693625	GM12878	blood:	n/a	n/a
16	BCL11A	chr12:10710317-10710684	GM12878	blood:	n/a	n/a
17	BCL11A	chr12:10696076-10696426	GM12878	blood:	n/a	n/a
18	BCL11A	chr12:10671811-10671985	GM12878	blood:	n/a	n/a
19	BCL11A	chr12:10693310-10693858	GM12878	blood:	n/a	n/a
20	BCL3	chr12:10696031-10696586	GM12878	blood:	n/a	n/a
21	BCL3	chr12:10693210-10693959	GM12878	blood:	n/a	n/a
22	BCL3	chr12:10695995-10696628	GM12878	blood:	n/a	n/a
23	BCL3	chr12:10693360-10693849	GM12878	blood:	n/a	n/a
24	BCL3	chr12:10711751-10712163	GM12878	blood:	n/a	chr12:10711876-10711885
25	BCL3	chr12:10710259-10710760	GM12878	blood:	n/a	chr12:10710710-10710719
26	BCLAF1	chr12:10714764-10715278	GM12878	blood:	n/a	chr12:10715136-10715145
27	BCLAF1	chr12:10693241-10693808	GM12878	blood:	n/a	n/a
28	BCLAF1	chr12:10707757-10708159	GM12878	blood:	n/a	n/a
29	BCLAF1	chr12:10693217-10694044	GM12878	blood:	n/a	n/a
30	BCLAF1	chr12:10696071-10696445	GM12878	blood:	n/a	n/a
31	BCLAF1	chr12:10709854-10710814	GM12878	blood:	n/a	chr12:10710710-10710719
32	BCLAF1	chr12:10706665-10707710	GM12878	blood:	n/a	n/a
33	BHLHE40	chr12:10710383-10710761	GM12878	blood:	n/a	n/a
34	BHLHE40	chr12:10693305-10693679	GM12878	blood:	n/a	n/a
35	BRCA1	chr12:10710053-10710128	GM12878	blood:	n/a	n/a
36	BRCA1	chr12:10676248-10676302	GM12878	blood:	n/a	n/a
37	CEBPB	chr12:10705717-10706316	GM12878	blood:	n/a	n/a
38	CEBPB	chr12:10693180-10693997	GM12878	blood:	n/a	n/a
39	CEBPB	chr12:10709894-10710828	GM12878	blood:	n/a	n/a
40	CEBPB	chr12:10675319-10675536	HepG2	liver:	n/a	chr12:10675436-10675447
41	CEBPB	chr12:10716337-10716441	HepG2	liver:	n/a	n/a
42	CEBPB	chr12:10706586-10708245	GM12878	blood:	n/a	n/a
43	CEBPB	chr12:10695688-10696520	GM12878	blood:	n/a	n/a
44	CEBPB	chr12:10675342-10675509	A549	lung:	n/a	chr12:10675436-10675447
45	CREB1	chr12:10693316-10693819	GM12878	blood:	n/a	n/a
46	CREB1	chr12:10693203-10694090	GM12878	blood:	n/a	n/a
47	CREB1	chr12:10674190-10674624	GM12878	blood:	n/a	n/a
48	CTCF	chr12:10711480-10711630	HRPEpiC	eye:	n/a	chr12:10711588-10711597 chr12:10711577-10711598 chr12:10711584-10711597 chr12:10711582-10711600
49	CTCF	chr12:10715040-10715190	HA-sp	spinal cord:	n/a	chr12:10715098-10715116 chr12:10715093-10715114 chr12:10715099-10715115 chr12:10715101-10715111
50	CTCF	chr12:10715300-10715450	Caco-2	colon:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10704318-10704368	NB4	blood:	n/a
2	chr12:10704009-10704059	HRCEpiC	kidney:	n/a
3	chr12:10704318-10704368	AG04449	skin:	fetal
4	chr12:10704318-10704368	HepG2	liver:	n/a
5	chr12:10704009-10704059	A549	lung:	n/a
6	chr12:10704318-10704368	SK-N-MC	brain:	n/a
7	chr12:10704009-10704059	T-47D	breast:	n/a
8	chr12:10704318-10704368	AG10803	skin:	n/a
9	chr12:10704074-10704124	HCPEpiC	choroid plexus:	n/a
10	chr12:10704318-10704368	HRPEpiC	eye:	n/a
11	chr12:10704009-10704059	NH-A	brain:	n/a
12	chr12:10704074-10704124	BJ	skin:	n/a
13	chr12:10704074-10704124	SK-N-SH_RA	brain:	n/a
14	chr12:10704318-10704368	HEEpiC	esophagus:	n/a
15	chr12:10704009-10704059	NHBE	bronchial:	n/a
16	chr12:10704009-10704059	GM06990	blood:	n/a
17	chr12:10704009-10704059	HRE	kidney:	n/a
18	chr12:10704318-10704368	HAEpiC	amniotic membrane:	n/a
19	chr12:10704318-10704368	GM12878	blood:	n/a
20	chr12:10704009-10704059	PANC-1	pancreas:	n/a
21	chr12:10704009-10704059	Jurkat	blood:	n/a
22	chr12:10704074-10704124	NT2-D1	testis:	n/a
23	chr12:10704074-10704124	HRCEpiC	kidney:	n/a
24	chr12:10704074-10704124	GM12878	blood:	n/a
25	chr12:10704074-10704124	LNCaP	prostate:	n/a
26	chr12:10704074-10704124	HIPEpiC	eye:	n/a
27	chr12:10704009-10704059	NHDF-neo	bronchial:	n/a
28	chr12:10704074-10704124	HNPCEpiC	eye:	n/a
29	chr12:10704074-10704124	HEEpiC	esophagus:	n/a
30	chr12:10704074-10704124	GM12891	blood:	n/a
31	chr12:10704074-10704124	ovcar-3	ovarian:	n/a
32	chr12:10704074-10704124	MCF-7	breast:	n/a
33	chr12:10704074-10704124	T-47D	breast:	n/a
34	chr12:10704009-10704059	HCT-116	colon:	n/a
35	chr12:10704009-10704059	HEEpiC	esophagus:	n/a
36	chr12:10704074-10704124	NH-A	brain:	n/a
37	chr12:10704074-10704124	HCF	heart:	n/a
38	chr12:10704074-10704124	HRPEpiC	eye:	n/a
39	chr12:10704009-10704059	ECC-1	luminal epithelium:	n/a
40	chr12:10704009-10704059	PFSK-1	brain:	n/a
41	chr12:10704009-10704059	PrEC	prostate:	n/a
42	chr12:10704074-10704124	GM19239	blood:	n/a
43	chr12:10704074-10704124	Jurkat	blood:	n/a
44	chr12:10704318-10704368	ECC-1	luminal epithelium:	n/a
45	chr12:10704318-10704368	SK-N-SH_RA	brain:	n/a
46	chr12:10704074-10704124	Hepatocyte	liver:	n/a
47	chr12:10704009-10704059	Caco-2	colon:	n/a
48	chr12:10704009-10704059	GM19239	blood:	n/a
49	chr12:10704009-10704059	HCM	heart:	n/a
50	chr12:10704009-10704059	HIPEpiC	eye:	n/a

(count:15 , 50 per page) page: 1

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

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

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

No data

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

Extended variants
information (count: 1808 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1808 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17809278	chr12:10663216-10663217	Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs4503631	chr12:10663265-10663266	Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs115407766	chr12:10663310-10663311	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs531489234	chr12:10663331-10663332	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs552140933	chr12:10663607-10663608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs565879011	chr12:10663610-10663611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs534782210	chr12:10663623-10663624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs186270361	chr12:10663781-10663782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138929538	chr12:10663794-10663795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs574547544	chr12:10663795-10663796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs561662945	chr12:10663846-10663847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537220477	chr12:10663860-10663861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs527284775	chr12:10663865-10663866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189173635	chr12:10663887-10663888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs547471645	chr12:10663893-10663894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs577051254	chr12:10663915-10663916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548413092	chr12:10663922-10663923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142658161	chr12:10663937-10663938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs138730225	chr12:10664051-10664052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573016729	chr12:10664086-10664087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs541956397	chr12:10664137-10664138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186633183	chr12:10664156-10664157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11053828	chr12:10664172-10664173	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs191743797	chr12:10664173-10664174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs73062509	chr12:10664250-10664251	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs7136822	chr12:10664332-10664333	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs146313263	chr12:10664334-10664335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs12299741	chr12:10664346-10664347	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs147880575	chr12:10664393-10664394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs555688697	chr12:10664418-10664419	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs148943849	chr12:10664437-10664438	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs149218826	chr12:10664468-10664469	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs568506736	chr12:10664471-10664472	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs536883438	chr12:10664475-10664476	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs56998430	chr12:10664476-10664477	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs577111886	chr12:10664481-10664482	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs541022521	chr12:10664487-10664488	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs539736092	chr12:10664488-10664489	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs181414134	chr12:10664521-10664522	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs534707252	chr12:10664545-10664546	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs371579953	chr12:10664555-10664556	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs557802217	chr12:10664566-10664567	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs73062510	chr12:10664643-10664644	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs35894489	chr12:10664674-10664675	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs541819579	chr12:10664695-10664696	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs561647154	chr12:10664708-10664709	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs148125591	chr12:10664741-10664742	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs141252444	chr12:10664747-10664748	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs77696742	chr12:10664774-10664775	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs532525321	chr12:10664818-10664819	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:209 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10663200-10663400	Bivalent/Poised TSS	Primary T helper memory cells from peripheral blood 1	blood
2	chr12:10663600-10665200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr12:10664400-10664800	Active TSS	Brain Hippocampus Middle	brain
4	chr12:10664600-10665000	Active TSS	Brain Anterior Caudate	brain
5	chr12:10664600-10665200	Enhancers	Brain Substantia Nigra	brain
6	chr12:10664800-10665000	Flanking Active TSS	Brain Hippocampus Middle	brain
7	chr12:10665000-10666200	Enhancers	Brain Hippocampus Middle	brain
8	chr12:10665200-10665600	Enhancers	Hela-S3	cervix
9	chr12:10674000-10674600	Enhancers	GM12878-XiMat	blood
10	chr12:10678000-10680800	Weak transcription	Fetal Intestine Small	intestine
11	chr12:10680200-10681000	Enhancers	Fetal Intestine Large	intestine
12	chr12:10680600-10680800	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr12:10680800-10681200	Active TSS	Duodenum Mucosa	Duodenum
14	chr12:10680800-10681200	Enhancers	Fetal Intestine Small	intestine
15	chr12:10680800-10681200	Active TSS	Rectal Mucosa Donor 29	rectum
16	chr12:10680800-10681200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
17	chr12:10680800-10681200	Enhancers	Sigmoid Colon	Sigmoid Colon
18	chr12:10681000-10681800	Weak transcription	Fetal Intestine Large	intestine
19	chr12:10681200-10681400	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr12:10681200-10681400	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr12:10681200-10682200	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr12:10681400-10681800	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr12:10681400-10682000	Enhancers	Rectal Mucosa Donor 29	rectum
24	chr12:10681800-10682600	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr12:10681800-10682800	Enhancers	Fetal Intestine Large	intestine
26	chr12:10682000-10682200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr12:10682000-10682400	Active TSS	Rectal Mucosa Donor 29	rectum
28	chr12:10682400-10682600	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr12:10682400-10682800	Enhancers	Rectal Mucosa Donor 29	rectum
30	chr12:10682400-10683600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr12:10683600-10684000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr12:10684000-10684400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
33	chr12:10684400-10684600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr12:10691000-10691800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr12:10691800-10693000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr12:10692800-10694200	Enhancers	Muscle Satellite Cultured Cells	--
37	chr12:10692800-10694600	Enhancers	GM12878-XiMat	blood
38	chr12:10693000-10694000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr12:10693000-10694200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr12:10693000-10694600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr12:10693000-10695000	Enhancers	NHDF-Ad	bronchial
42	chr12:10693200-10694000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr12:10693200-10694000	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr12:10693200-10694000	Enhancers	Dnd41	blood
45	chr12:10693200-10694000	Enhancers	HMEC	breast
46	chr12:10693200-10694000	Enhancers	NHEK	skin
47	chr12:10693200-10694200	Enhancers	Osteobl	bone
48	chr12:10693400-10694000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr12:10693400-10694000	Enhancers	HSMM	muscle
50	chr12:10693600-10694000	Enhancers	Thymus	Thymus

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