Variant report

Variant	nsv508628
Chromosome Location	chr11:48274154-48359743
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:48356437-48356637	K562	blood:	n/a	n/a
2	ATF1	chr11:48292484-48292679	K562	blood:	n/a	n/a
3	BACH1	chr11:48356973-48356986	K562	blood:	n/a	n/a
4	BRCA1	chr11:48329323-48329679	Hela-S3	cervix:	n/a	n/a
5	CBX3	chr11:48329320-48329744	HCT-116	colon:	n/a	n/a
6	CEBPB	chr11:48340990-48341301	A549	lung:	n/a	n/a
7	CEBPB	chr11:48332469-48332671	HepG2	liver:	n/a	chr11:48332598-48332609
8	CHD2	chr11:48344566-48344658	K562	blood:	n/a	n/a
9	CTCF	chr11:48329784-48329877	GM10266	blood:	n/a	n/a
10	CTCF	chr11:48329440-48329590	GM12864	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
11	CTCF	chr11:48329400-48329550	HRPEpiC	eye:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
12	CTCF	chr11:48329440-48329590	HRE	kidney:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
13	CTCF	chr11:48329352-48329668	Medullo	brain:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
14	CTCF	chr11:48329152-48329946	SK-N-SH	brain:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
15	CTCF	chr11:48326940-48327090	GM12864	blood:	n/a	n/a
16	CTCF	chr11:48329396-48329572	H1-hESC	embryonic stem cell:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
17	CTCF	chr11:48347233-48347255	Fibrobl	skin:	n/a	n/a
18	CTCF	chr11:48329360-48329510	HFF-Myc	foreskin:	n/a	n/a
19	CTCF	chr11:48329400-48329550	GM12871	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
20	CTCF	chr11:48342180-48342330	AoAF	blood vessel:	n/a	n/a
21	CTCF	chr11:48329440-48329590	BE2_C	brain:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
22	CTCF	chr11:48329440-48329590	GM12875	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
23	CTCF	chr11:48329460-48329610	GM12870	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
24	CTCF	chr11:48329386-48329605	MCF-7	breast:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
25	CTCF	chr11:48329382-48329751	K562	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
26	CTCF	chr11:48329420-48329570	GM12868	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
27	CTCF	chr11:48320420-48320570	GM12871	blood:	n/a	n/a
28	CTCF	chr11:48329300-48329450	WI-38	lung:	n/a	n/a
29	CTCF	chr11:48329440-48329590	HepG2	liver:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
30	CTCF	chr11:48329460-48329610	NHLF	lung:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
31	CTCF	chr11:48329180-48329829	MCF-7	breast:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
32	CTCF	chr11:48329320-48329756	HCT-116	colon:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
33	CTCF	chr11:48329420-48329570	AG09309	skin:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
34	CTCF	chr11:48329460-48329610	HCM	heart:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
35	CTCF	chr11:48329420-48329570	GM12873	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
36	CTCF	chr11:48329274-48329773	T-47D	breast:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
37	CTCF	chr11:48329360-48329510	HVMF	connective:	n/a	n/a
38	CTCF	chr11:48329343-48329665	MCF-7	breast:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
39	CTCF	chr11:48329440-48329590	GM12872	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
40	CTCF	chr11:48329460-48329610	AG04450	lung:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
41	CTCF	chr11:48297227-48297276	LNCaP	prostate:	n/a	n/a
42	CTCF	chr11:48329440-48329590	HPAF	blood vessel:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
43	CTCF	chr11:48329440-48329590	HVMF	connective:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
44	CTCF	chr11:48329440-48329590	MCF-7	breast:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
45	CTCF	chr11:48329383-48329628	GM13976	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
46	CTCF	chr11:48329420-48329570	GM12869	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
47	CTCF	chr11:48329440-48329590	AG09309	skin:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
48	CTCF	chr11:48329440-48329590	GM12878	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
49	CTCF	chr11:48329420-48329570	GM12865	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
50	CTCF	chr11:48329460-48329610	GM12865	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48328132-48328182	HPAEpiC	pulmonary alveolar:	n/a
2	chr11:48345361-48345411	LNCaP	prostate:	n/a
3	chr11:48285200-48285250	SKMC	muscle:	n/a
4	chr11:48346680-48346730	GM06990	blood:	n/a
5	chr11:48284249-48284299	HCT-116	colon:	n/a
6	chr11:48345361-48345411	AG04449	skin:	fetal
7	chr11:48328132-48328182	MCF10A-Er-Src	breast:	n/a
8	chr11:48345815-48345865	NHDF-neo	bronchial:	n/a
9	chr11:48284249-48284299	HPAEpiC	pulmonary alveolar:	n/a
10	chr11:48328132-48328182	HCF	heart:	n/a
11	chr11:48326388-48326438	GM12892	blood:	n/a
12	chr11:48285821-48285871	H1-hESC	embryonic stem cell:	embryo
13	chr11:48345361-48345411	NT2-D1	testis:	n/a
14	chr11:48345815-48345865	SK-N-MC	brain:	n/a
15	chr11:48285821-48285871	A549	lung:	n/a
16	chr11:48328132-48328182	CMK	blood:	n/a
17	chr11:48345815-48345865	HEK293	kidney:	embryo
18	chr11:48285821-48285871	NB4	blood:	n/a
19	chr11:48346680-48346730	SKMC	muscle:	n/a
20	chr11:48284249-48284299	SKMC	muscle:	n/a
21	chr11:48345815-48345865	NHBE	bronchial:	n/a
22	chr11:48346680-48346730	HEEpiC	esophagus:	n/a
23	chr11:48346680-48346730	NT2-D1	testis:	n/a
24	chr11:48327164-48327214	AG04450	lung:	fetal
25	chr11:48327164-48327214	HCPEpiC	choroid plexus:	n/a
26	chr11:48345815-48345865	BE2_C	brain:	n/a
27	chr11:48346680-48346730	NHDF-neo	bronchial:	n/a
28	chr11:48285200-48285250	NT2-D1	testis:	n/a
29	chr11:48285821-48285871	ECC-1	luminal epithelium:	n/a
30	chr11:48284249-48284299	LNCaP	prostate:	n/a
31	chr11:48328132-48328182	GM12878	blood:	n/a
32	chr11:48327164-48327214	SK-N-SH_RA	brain:	n/a
33	chr11:48345361-48345411	PFSK-1	brain:	n/a
34	chr11:48345815-48345865	HCF	heart:	n/a
35	chr11:48327164-48327214	AG04449	skin:	fetal
36	chr11:48346680-48346730	A549	lung:	n/a
37	chr11:48345361-48345411	CMK	blood:	n/a
38	chr11:48345361-48345411	HEK293	kidney:	embryo
39	chr11:48285200-48285250	HCM	heart:	n/a
40	chr11:48346680-48346730	GM12892	blood:	n/a
41	chr11:48326388-48326438	HRCEpiC	kidney:	n/a
42	chr11:48284249-48284299	SK-N-SH_RA	brain:	n/a
43	chr11:48346680-48346730	MCF10A-Er-Src	breast:	n/a
44	chr11:48345815-48345865	NT2-D1	testis:	n/a
45	chr11:48284249-48284299	HCM	heart:	n/a
46	chr11:48328132-48328182	Caco-2	colon:	n/a
47	chr11:48345815-48345865	ovcar-3	ovarian:	n/a
48	chr11:48345361-48345411	AG09319	gingival:	n/a
49	chr11:48285821-48285871	NHBE	bronchial:	n/a
50	chr11:48345361-48345411	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:48234220..48234962-chr11:48329425..48329937,2	MCF-7	breast:
2	chr11:48292794..48294613-chr11:48297509..48299435,2	K562	blood:
3	chr11:48292794..48294613-chr11:48297509..48299435,2	K562	blood:

Variant related genes	Relation type
OR4X1	TF binding region
OR4C3	TF binding region
OR4S1	TF binding region
OR4X1	CpG island
OR4C3	CpG island
OR4S1	CpG island

Extended variants
information (count: 2285 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2285 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562507889	chr11:48283008-48283009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs563532124	chr11:48283036-48283037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531606028	chr11:48283038-48283039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141551969	chr11:48283060-48283061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs550802551	chr11:48283088-48283089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs150393331	chr11:48283147-48283148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561019310	chr11:48283189-48283190	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs188314050	chr11:48283212-48283213	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs377162135	chr11:48283239-48283240	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs138232057	chr11:48283242-48283243	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs149159407	chr11:48283274-48283275	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs7106648	chr11:48283292-48283293	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs546460780	chr11:48283298-48283299	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs372494317	chr11:48283299-48283300	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs375625655	chr11:48283309-48283310	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs143149750	chr11:48283313-48283314	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs368658923	chr11:48283335-48283336	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs563934311	chr11:48283344-48283345	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs77064443	chr11:48283470-48283471	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs546920730	chr11:48283501-48283502	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs375932029	chr11:48283506-48283507	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs567031477	chr11:48283525-48283526	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs138661459	chr11:48283556-48283557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372667371	chr11:48283577-48283578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs531344264	chr11:48283597-48283598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs559056035	chr11:48283608-48283609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569280709	chr11:48283696-48283697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538195286	chr11:48283700-48283701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs202014078	chr11:48283701-48283702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369257249	chr11:48283760-48283761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs1393797	chr11:48283763-48283764	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs542891358	chr11:48283793-48283794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191996970	chr11:48283802-48283803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs572966072	chr11:48283808-48283809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs34290179	chr11:48283811-48283812	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs564597831	chr11:48283827-48283828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530429931	chr11:48283877-48283878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs538705240	chr11:48283918-48283919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560539415	chr11:48283937-48283938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs12807125	chr11:48283979-48283980	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs141905088	chr11:48283980-48283981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs1109905	chr11:48284000-48284001	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs145566588	chr11:48284009-48284010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552705182	chr11:48284017-48284018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183874159	chr11:48284020-48284021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs1109906	chr11:48284033-48284034	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs555036267	chr11:48284083-48284084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs2870509	chr11:48284109-48284110	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs571049160	chr11:48284110-48284111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs905483	chr11:48284139-48284140	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	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
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Breast cancer	21990379	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48283000-48285000	Enhancers	GM12878-XiMat	blood
2	chr11:48288800-48289000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr11:48293400-48294200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
4	chr11:48293600-48294200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
5	chr11:48294000-48294400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
6	chr11:48294400-48295000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
7	chr11:48294800-48295200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
8	chr11:48295000-48295200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
9	chr11:48314000-48314400	Active TSS	ES-I3 Cell Line	embryonic stem cell
10	chr11:48328000-48328400	Enhancers	Lung	lung
11	chr11:48329400-48329800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
12	chr11:48329400-48330000	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr11:48329600-48329800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
14	chr11:48329600-48329800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr11:48329600-48329800	Enhancers	Brain Angular Gyrus	brain
16	chr11:48329600-48329800	Enhancers	Brain Cingulate Gyrus	brain
17	chr11:48329600-48329800	Enhancers	Brain Hippocampus Middle	brain
18	chr11:48336400-48337600	Enhancers	Stomach Mucosa	stomach
19	chr11:48337600-48341200	Weak transcription	Stomach Mucosa	stomach
20	chr11:48341200-48342600	Enhancers	Stomach Mucosa	stomach
21	chr11:48341400-48345800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
22	chr11:48341600-48341800	Bivalent Enhancer	Left Ventricle	heart
23	chr11:48341600-48342000	Bivalent Enhancer	Right Atrium	heart
24	chr11:48341600-48342000	Enhancers	Spleen	Spleen
25	chr11:48341800-48342000	Enhancers	Left Ventricle	heart
26	chr11:48342600-48344400	Weak transcription	Stomach Mucosa	stomach
27	chr11:48344400-48344800	Enhancers	Stomach Mucosa	stomach
28	chr11:48344800-48349800	Weak transcription	Stomach Mucosa	stomach
29	chr11:48346600-48346800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr11:48346600-48347000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
31	chr11:48346600-48347400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr11:48346600-48348600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr11:48346800-48347400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr11:48348800-48350000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr11:48350000-48355600	Weak transcription	Stomach Mucosa	stomach
36	chr11:48352400-48353400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
37	chr11:48352400-48353800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
38	chr11:48353000-48359800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
39	chr11:48355200-48363800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
40	chr11:48355600-48357000	Enhancers	Stomach Mucosa	stomach
41	chr11:48357000-48358000	Weak transcription	Stomach Mucosa	stomach
42	chr11:48358000-48358200	Enhancers	Stomach Mucosa	stomach

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