Variant report

Variant	nsv7676
Chromosome Location	chr11:10689144-10734139
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:380)
CpG islands
(count:1037)
Chromatin interactive
region (count:54)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:380 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:10703093-10703162	K562	blood:	n/a	n/a
2	ATF1	chr11:10717629-10717789	K562	blood:	n/a	n/a
3	BHLHE40	chr11:10696710-10697109	K562	blood:	n/a	chr11:10696899-10696908
4	BHLHE40	chr11:10696768-10697055	HepG2	liver:	n/a	chr11:10696899-10696908
5	BHLHE40	chr11:10709933-10710175	K562	blood:	n/a	n/a
6	BHLHE40	chr11:10696825-10697022	GM12878	blood:	n/a	chr11:10696899-10696908
7	BRCA1	chr11:10689000-10689289	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr11:10690363-10692064	HCT-116	colon:	n/a	n/a
9	CBX3	chr11:10720723-10721049	K562	blood:	n/a	n/a
10	CEBPB	chr11:10697141-10697249	HepG2	liver:	n/a	chr11:10697190-10697201
11	CEBPB	chr11:10720716-10720736	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr11:10728957-10729000	K562	blood:	n/a	n/a
13	CEBPB	chr11:10723263-10723462	A549	lung:	n/a	chr11:10723371-10723384 chr11:10723351-10723362 chr11:10723371-10723382
14	CEBPB	chr11:10723263-10723511	HepG2	liver:	n/a	chr11:10723371-10723384 chr11:10723351-10723362 chr11:10723371-10723382
15	CEBPB	chr11:10720621-10720888	IMR90	lung:	n/a	n/a
16	CEBPB	chr11:10720721-10720747	K562	blood:	n/a	n/a
17	CEBPB	chr11:10688994-10689383	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr11:10720712-10720724	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr11:10690829-10691620	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr11:10720621-10720861	A549	lung:	n/a	n/a
21	CTCF	chr11:10710000-10710150	GM12872	blood:	n/a	n/a
22	CTCF	chr11:10716480-10716630	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr11:10709907-10710242	K562	blood:	n/a	n/a
24	CTCF	chr11:10710020-10710170	HMF	breast:	n/a	n/a
25	CTCF	chr11:10709960-10710110	GM12865	blood:	n/a	n/a
26	CTCF	chr11:10709980-10710130	AG10803	skin:	n/a	n/a
27	CTCF	chr11:10710000-10710150	GM12865	blood:	n/a	n/a
28	CTCF	chr11:10720200-10720350	RPTEC	kidney:	n/a	n/a
29	CTCF	chr11:10716460-10716610	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr11:10709960-10710110	AoAF	blood vessel:	n/a	n/a
31	CTCF	chr11:10710110-10710115	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr11:10709960-10710110	HCM	heart:	n/a	n/a
33	CTCF	chr11:10716480-10716630	HepG2	liver:	n/a	n/a
34	CTCF	chr11:10720180-10720330	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr11:10709980-10710130	BJ	skin:	n/a	n/a
36	CTCF	chr11:10723560-10723710	NHEK	skin:	n/a	n/a
37	CTCF	chr11:10716480-10716630	HMF	breast:	n/a	n/a
38	CTCF	chr11:10709900-10710050	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr11:10709920-10710070	HPF	lung:	n/a	n/a
40	CTCF	chr11:10690820-10690970	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr11:10709980-10710130	WI-38	lung:	n/a	n/a
42	CTCF	chr11:10709999-10710135	MCF-7	breast:	n/a	n/a
43	CTCF	chr11:10715100-10715250	AG04449	skin:	n/a	n/a
44	CTCF	chr11:10716500-10716650	HPF	lung:	n/a	n/a
45	CTCF	chr11:10709960-10710110	AG09309	skin:	n/a	n/a
46	CTCF	chr11:10709840-10709990	GM12869	blood:	n/a	n/a
47	CTCF	chr11:10709720-10709870	GM12875	blood:	n/a	n/a
48	CTCF	chr11:10720160-10720310	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr11:10716480-10716630	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr11:10710040-10710190	GM12872	blood:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:10715360-10715410	HCF	heart:	n/a
2	chr11:10715217-10715267	NHBE	bronchial:	n/a
3	chr11:10715715-10715765	HL-60	blood:	n/a
4	chr11:10715175-10715225	SKMC	muscle:	n/a
5	chr11:10715571-10715621	GM12891	blood:	n/a
6	chr11:10715221-10715271	U87	brain:	n/a
7	chr11:10715360-10715410	HCM	heart:	n/a
8	chr11:10715571-10715621	HPAEpiC	pulmonary alveolar:	n/a
9	chr11:10715571-10715621	HRCEpiC	kidney:	n/a
10	chr11:10715767-10715817	AG09309	skin:	n/a
11	chr11:10715175-10715225	HCM	heart:	n/a
12	chr11:10715445-10715495	PFSK-1	brain:	n/a
13	chr11:10703262-10703312	AG09309	skin:	n/a
14	chr11:10715217-10715267	AG04450	lung:	fetal
15	chr11:10715188-10715238	Caco-2	colon:	n/a
16	chr11:10715360-10715410	U87	brain:	n/a
17	chr11:10715188-10715238	HCF	heart:	n/a
18	chr11:10715221-10715271	NB4	blood:	n/a
19	chr11:10715213-10715263	CMK	blood:	n/a
20	chr11:10715571-10715621	NHBE	bronchial:	n/a
21	chr11:10730185-10730235	ECC-1	luminal epithelium:	n/a
22	chr11:10715595-10715645	HL-60	blood:	n/a
23	chr11:10716164-10716214	ovcar-3	ovarian:	n/a
24	chr11:10730185-10730235	Jurkat	blood:	n/a
25	chr11:10730185-10730235	Hepatocyte	liver:	n/a
26	chr11:10716164-10716214	U87	brain:	n/a
27	chr11:10715175-10715225	AG10803	skin:	n/a
28	chr11:10715445-10715495	NHDF-neo	bronchial:	n/a
29	chr11:10715445-10715495	MCF10A-Er-Src	breast:	n/a
30	chr11:10715767-10715817	HAEpiC	amniotic membrane:	n/a
31	chr11:10730185-10730235	HNPCEpiC	eye:	n/a
32	chr11:10716164-10716214	HIPEpiC	eye:	n/a
33	chr11:10703262-10703312	T-47D	breast:	n/a
34	chr11:10730185-10730235	Caco-2	colon:	n/a
35	chr11:10715715-10715765	K562	blood:	n/a
36	chr11:10715360-10715410	ECC-1	luminal epithelium:	n/a
37	chr11:10715213-10715263	Hela-S3	cervix:	n/a
38	chr11:10715360-10715410	HEEpiC	esophagus:	n/a
39	chr11:10715571-10715621	AoSMC	blood vessel:	n/a
40	chr11:10715213-10715263	PrEC	prostate:	n/a
41	chr11:10715217-10715267	HL-60	blood:	n/a
42	chr11:10703262-10703312	AG04450	lung:	fetal
43	chr11:10716164-10716214	HPAEpiC	pulmonary alveolar:	n/a
44	chr11:10715217-10715267	HCPEpiC	choroid plexus:	n/a
45	chr11:10715715-10715765	AG04450	lung:	fetal
46	chr11:10703262-10703312	Hepatocyte	liver:	n/a
47	chr11:10715445-10715495	NT2-D1	testis:	n/a
48	chr11:10716455-10716505	Hepatocyte	liver:	n/a
49	chr11:10715767-10715817	GM06990	blood:	n/a
50	chr11:10715175-10715225	HEEpiC	esophagus:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:10689514..10690158-chr5:36806169..36807035,2	MCF-7	breast:
2	chr11:10689241..10690956-chr11:10698574..10700529,2	K562	blood:
3	chr11:10709131..10712836-chr11:10712999..10717374,5	K562	blood:
4	chr11:10690159..10692528-chr11:10735582..10739094,3	MCF-7	breast:
5	chr11:10699841..10701400-chr11:10708339..10710277,2	K562	blood:
6	chr11:10679397..10680975-chr11:10707592..10709737,2	K562	blood:
7	chr11:10731860..10733489-chr11:10733521..10735446,2	K562	blood:
8	chr11:10693377..10695565-chr11:10697509..10699957,3	K562	blood:
9	chr11:10589192..10591636-chr11:10696263..10698924,2	K562	blood:
10	chr11:10699841..10701400-chr11:10708339..10710277,2	K562	blood:
11	chr11:10688907..10690488-chr11:10693556..10695062,2	K562	blood:
12	chr11:10728663..10731257-chr11:10732876..10735341,4	K562	blood:
13	chr11:10699670..10701263-chr11:10703402..10706052,2	K562	blood:
14	chr11:10694517..10697367-chr11:10731815..10734225,2	K562	blood:
15	chr11:10628715..10631379-chr11:10733755..10736370,2	K562	blood:
16	chr11:10692446..10695017-chr11:10698457..10700738,2	K562	blood:
17	chr11:10678525..10679388-chr11:10716241..10717042,2	K562	blood:
18	chr11:10699670..10701867-chr11:10703402..10705803,2	K562	blood:
19	chr11:10704355..10706208-chr11:10708118..10710212,2	K562	blood:
20	chr11:10699670..10701263-chr11:10703402..10706052,2	K562	blood:
21	chr11:10689241..10690956-chr11:10698574..10700529,2	K562	blood:
22	chr11:10728663..10731257-chr11:10732876..10735341,4	K562	blood:
23	chr11:10689604..10691853-chr11:10718013..10720548,2	K562	blood:
24	chr11:10689604..10691853-chr11:10718013..10720548,2	K562	blood:
25	chr11:10726070..10727726-chr11:10756782..10759046,2	K562	blood:
26	chr11:10688135..10690797-chr11:10695097..10696777,2	K562	blood:
27	chr11:10681198..10682057-chr11:10690650..10691471,2	HCT-116	colon:
28	chr11:10476408..10478780-chr11:10703705..10706563,2	K562	blood:
29	chr11:10691286..10695244-chr11:10695981..10700197,4	MCF-7	breast:
30	chr11:10688907..10690488-chr11:10693556..10695062,2	K562	blood:
31	chr11:10691286..10695244-chr11:10695981..10700197,4	MCF-7	breast:
32	chr11:10709263..10710833-chr11:10780205..10782921,2	K562	blood:
33	chr11:10699670..10701867-chr11:10703402..10705803,2	K562	blood:
34	chr11:10714480..10714980-chr2:10183367..10183928,2	MCF-7	breast:
35	chr11:10733667..10735565-chr11:10738742..10741384,2	K562	blood:
36	chr11:10731860..10733489-chr11:10733521..10735446,2	K562	blood:
37	chr11:10710338..10712836-chr11:10714541..10717374,3	K562	blood:
38	chr11:10690084..10691721-chr11:10696494..10698749,2	K562	blood:
39	chr11:10721902..10723724-chr11:10731572..10734074,2	MCF-7	breast:
40	chr11:10703793..10706568-chr11:10708118..10712045,4	K562	blood:
41	chr11:10703793..10706568-chr11:10708118..10712045,4	K562	blood:
42	chr11:10687959..10690834-chr11:10758767..10760971,2	K562	blood:
43	chr11:10694517..10697367-chr11:10731815..10734225,2	K562	blood:
44	chr11:10704355..10706208-chr11:10708118..10710212,2	K562	blood:
45	chr11:10702876..10705073-chr11:10754687..10757563,2	K562	blood:
46	chr11:10690084..10691721-chr11:10696494..10698749,2	K562	blood:
47	chr11:10679153..10681988-chr11:10698825..10701306,2	K562	blood:
48	chr11:10721902..10723724-chr11:10731572..10734074,2	MCF-7	breast:
49	chr11:10688135..10690797-chr11:10695097..10696777,2	K562	blood:
50	chr11:10692446..10695017-chr11:10698457..10700738,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LYVE1-1	chr11:10715083-10715351	NONHSAT017978
2	lnc-LYVE1-1	chr11:10715367-10715504	NONHSAT017977

No data

Variant related genes	Relation type
MRVI1	TF binding region
MRVI1	CpG island
ENSG00000173557	chromatin interactions
ENSG00000198730	chromatin interactions
ENSG00000072952	chromatin interactions
ENSG00000172059	chromatin interactions
ENSG00000133805	chromatin interactions
ENSG00000133800	chromatin interactions

Extended variants
information (count: 1752 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1752 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115018783	chr11:10689164-10689165	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs559768535	chr11:10689223-10689224	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs903822	chr11:10689226-10689227	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs548296742	chr11:10689229-10689230	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs537990316	chr11:10689233-10689234	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs881870	chr11:10689262-10689263	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs117031137	chr11:10689277-10689278	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs376857671	chr11:10689322-10689323	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs372057209	chr11:10689343-10689344	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs190333054	chr11:10689381-10689382	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs881869	chr11:10689454-10689455	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs192458186	chr11:10689455-10689456	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs535380657	chr11:10689464-10689465	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs372918028	chr11:10689468-10689469	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs79801174	chr11:10689570-10689571	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575482927	chr11:10689586-10689587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560200819	chr11:10689600-10689601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557961428	chr11:10689602-10689603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573631074	chr11:10689603-10689604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149007500	chr11:10689647-10689648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs202193404	chr11:10689648-10689649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs115576281	chr11:10689670-10689671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs559856239	chr11:10689709-10689710	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76573573	chr11:10689738-10689739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535192738	chr11:10689766-10689767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74938088	chr11:10689767-10689768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs1390571	chr11:10689820-10689821	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs117595272	chr11:10689827-10689828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113518697	chr11:10689835-10689836	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148326673	chr11:10689976-10689977	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185060389	chr11:10689994-10689995	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546796353	chr11:10690023-10690024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376014234	chr11:10690033-10690034	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528432849	chr11:10690071-10690072	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs79671632	chr11:10690092-10690093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568785945	chr11:10690099-10690100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538128227	chr11:10690101-10690102	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558049786	chr11:10690134-10690135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113353104	chr11:10690156-10690157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs71965271	chr11:10690211-10690212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533934752	chr11:10690226-10690227	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111275391	chr11:10690227-10690228	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1390572	chr11:10690257-10690258	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs541987358	chr11:10690267-10690268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138286503	chr11:10690300-10690301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs370789171	chr11:10690328-10690329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188258888	chr11:10690342-10690343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550734824	chr11:10690443-10690444	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs564356654	chr11:10690521-10690522	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs181057572	chr11:10690548-10690549	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Neuroblastoma	18923524	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:948 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:10674600-10689600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr11:10680600-10696200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:10682200-10690400	Weak transcription	Duodenum Mucosa	Duodenum
4	chr11:10683800-10692400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr11:10684400-10692000	Enhancers	Ovary	ovary
6	chr11:10684800-10689200	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr11:10685000-10689200	Enhancers	Brain Anterior Caudate	brain
8	chr11:10685000-10690800	Enhancers	NHDF-Ad	bronchial
9	chr11:10686000-10690400	Weak transcription	Spleen	Spleen
10	chr11:10686000-10692200	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr11:10686200-10690400	Weak transcription	Fetal Intestine Small	intestine
12	chr11:10686200-10690400	Weak transcription	Placenta	Placenta
13	chr11:10686400-10690400	Enhancers	Colon Smooth Muscle	Colon
14	chr11:10686400-10690400	Weak transcription	Right Ventricle	heart
15	chr11:10686800-10689800	Enhancers	K562	blood
16	chr11:10686800-10691400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr11:10687200-10689600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr11:10687200-10692000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr11:10687400-10689800	Enhancers	Aorta	Aorta
20	chr11:10687400-10690400	Enhancers	Rectal Smooth Muscle	rectum
21	chr11:10687400-10691000	Enhancers	NHLF	lung
22	chr11:10687400-10691400	Enhancers	Placenta Amnion	Placenta Amnion
23	chr11:10687600-10689400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr11:10687600-10690400	Weak transcription	Lung	lung
25	chr11:10687600-10690400	Weak transcription	Small Intestine	intestine
26	chr11:10687600-10690800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr11:10687600-10691800	Enhancers	Osteobl	bone
28	chr11:10687800-10689400	Enhancers	NH-A	brain
29	chr11:10687800-10689800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr11:10687800-10689800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr11:10687800-10690400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr11:10687800-10690800	Enhancers	Hela-S3	cervix
33	chr11:10688000-10689200	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr11:10688000-10689200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr11:10688000-10689400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr11:10688000-10689400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr11:10688000-10690000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr11:10688000-10691000	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr11:10688000-10692200	Enhancers	HSMMtube	muscle
40	chr11:10688200-10689200	Enhancers	Primary hematopoietic stem cells	blood
41	chr11:10688200-10691600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr11:10688200-10691800	Enhancers	Brain Hippocampus Middle	brain
43	chr11:10688200-10692000	Enhancers	Adipose Nuclei	Adipose
44	chr11:10688200-10692200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr11:10688200-10692200	Enhancers	HSMM	muscle
46	chr11:10688400-10689200	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr11:10688400-10689600	Weak transcription	Brain Angular Gyrus	brain
48	chr11:10688400-10689800	Enhancers	Fetal Muscle Leg	muscle
49	chr11:10688400-10692200	Enhancers	Duodenum Smooth Muscle	Duodenum
50	chr11:10688600-10690400	Weak transcription	Skeletal Muscle Male	skeletal muscle

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