Variant report

Variant	nsv1041394
Chromosome Location	chr11:48188748-48346202
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	ARID3A	chr11:48194471-48194702	HepG2	liver:	n/a	n/a
2	ATF1	chr11:48292484-48292679	K562	blood:	n/a	n/a
3	ATF3	chr11:48194364-48194613	K562	blood:	n/a	n/a
4	ATF3	chr11:48194480-48194676	K562	blood:	n/a	n/a
5	BHLHE40	chr11:48194470-48194703	GM12878	blood:	n/a	n/a
6	BRCA1	chr11:48329323-48329679	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr11:48194475-48194742	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr11:48235490-48235559	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr11:48194532-48194633	GM12878	blood:	n/a	n/a
10	CBX3	chr11:48329320-48329744	HCT-116	colon:	n/a	n/a
11	CEBPB	chr11:48232372-48232647	Hela-S3	cervix:	n/a	chr11:48232504-48232515
12	CEBPB	chr11:48194408-48194759	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr11:48332469-48332671	HepG2	liver:	n/a	chr11:48332598-48332609
14	CEBPB	chr11:48232376-48232660	HepG2	liver:	n/a	chr11:48232504-48232515
15	CEBPB	chr11:48232368-48232629	A549	lung:	n/a	chr11:48232504-48232515
16	CEBPB	chr11:48232351-48232666	K562	blood:	n/a	chr11:48232504-48232515
17	CEBPB	chr11:48340990-48341301	A549	lung:	n/a	n/a
18	CEBPB	chr11:48232346-48232660	IMR90	lung:	n/a	chr11:48232504-48232515
19	CHD1	chr11:48194544-48194553	GM12878	blood:	n/a	n/a
20	CHD2	chr11:48212930-48213130	K562	blood:	n/a	n/a
21	CHD2	chr11:48194572-48194700	HepG2	liver:	n/a	n/a
22	CHD2	chr11:48344566-48344658	K562	blood:	n/a	n/a
23	CHD2	chr11:48199898-48199928	Hela-S3	cervix:	n/a	n/a
24	CREB1	chr11:48194478-48194746	A549	lung:	n/a	n/a
25	CTCF	chr11:48329460-48329610	GM12868	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
26	CTCF	chr11:48194520-48194670	GM12869	blood:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
27	CTCF	chr11:48329460-48329610	AG10803	skin:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
28	CTCF	chr11:48194361-48195010	SK-N-SH	brain:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194723-48194736 chr11:48194575-48194588 chr11:48194573-48194589
29	CTCF	chr11:48194387-48194752	K562	blood:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194723-48194736 chr11:48194575-48194588 chr11:48194573-48194589
30	CTCF	chr11:48329360-48329510	HVMF	connective:	n/a	n/a
31	CTCF	chr11:48194500-48194650	GM12868	blood:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
32	CTCF	chr11:48194411-48194719	Lung_OC	lung:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
33	CTCF	chr11:48231720-48231870	MCF-7	breast:	n/a	n/a
34	CTCF	chr11:48194403-48194736	GM12878	blood:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194723-48194736 chr11:48194575-48194588 chr11:48194573-48194589
35	CTCF	chr11:48206098-48206211	LNCaP	prostate:	n/a	chr11:48206171-48206192
36	CTCF	chr11:48194500-48194650	SK-N-SH_RA	brain:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
37	CTCF	chr11:48194401-48194729	Gliobla	brain:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
38	CTCF	chr11:48194460-48194610	GM12875	blood:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
39	CTCF	chr11:48326840-48326990	SAEC	small airway:	n/a	n/a
40	CTCF	chr11:48194371-48194699	H1-hESC	embryonic stem cell:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
41	CTCF	chr11:48329365-48329661	GM13977	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
42	CTCF	chr11:48194406-48194806	HCT-116	colon:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194723-48194736 chr11:48194575-48194588 chr11:48194573-48194589
43	CTCF	chr11:48234435-48234479	LNCaP	prostate:	n/a	chr11:48234443-48234464
44	CTCF	chr11:48231680-48231830	GM12868	blood:	n/a	n/a
45	CTCF	chr11:48329440-48329590	BE2_C	brain:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
46	CTCF	chr11:48329460-48329610	GM12878	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
47	CTCF	chr11:48206140-48206290	MCF-7	breast:	n/a	chr11:48206171-48206192
48	CTCF	chr11:48194520-48194670	HCM	heart:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
49	CTCF	chr11:48194416-48194714	GM10266	blood:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
50	CTCF	chr11:48231680-48231830	HCT-116	colon:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48326388-48326438	AG09309	skin:	n/a
2	chr11:48326388-48326438	AG09309	skin:	n/a
3	chr11:48238296-48238346	SK-N-SH_RA	brain:	n/a
4	chr11:48327164-48327214	AG09319	gingival:	n/a
5	chr11:48238724-48238774	ECC-1	luminal epithelium:	n/a
6	chr11:48191068-48191118	HCM	heart:	n/a
7	chr11:48237353-48237403	NHDF-neo	bronchial:	n/a
8	chr11:48327164-48327214	CMK	blood:	n/a
9	chr11:48237353-48237403	HNPCEpiC	eye:	n/a
10	chr11:48266856-48266906	HRPEpiC	eye:	n/a
11	chr11:48191068-48191118	K562	blood:	n/a
12	chr11:48238724-48238774	HPAEpiC	pulmonary alveolar:	n/a
13	chr11:48238724-48238774	HL-60	blood:	n/a
14	chr11:48238724-48238774	AG09309	skin:	n/a
15	chr11:48345361-48345411	H1-hESC	embryonic stem cell:	embryo
16	chr11:48328132-48328182	ovcar-3	ovarian:	n/a
17	chr11:48238724-48238774	HAEpiC	amniotic membrane:	n/a
18	chr11:48238724-48238774	K562	blood:	n/a
19	chr11:48266856-48266906	ProgFib	skin:	n/a
20	chr11:48191068-48191118	HCT-116	colon:	n/a
21	chr11:48285200-48285250	AG04450	lung:	fetal
22	chr11:48345815-48345865	HCM	heart:	n/a
23	chr11:48191068-48191118	AG04450	lung:	fetal
24	chr11:48285200-48285250	GM06990	blood:	n/a
25	chr11:48238296-48238346	Jurkat	blood:	n/a
26	chr11:48327164-48327214	NB4	blood:	n/a
27	chr11:48284249-48284299	BE2_C	brain:	n/a
28	chr11:48285821-48285871	PrEC	prostate:	n/a
29	chr11:48237358-48237408	NH-A	brain:	n/a
30	chr11:48326388-48326438	IMR90	lung:	fetal
31	chr11:48345815-48345865	U87	brain:	n/a
32	chr11:48191068-48191118	AoSMC	blood vessel:	n/a
33	chr11:48266856-48266906	ovcar-3	ovarian:	n/a
34	chr11:48326388-48326438	HRPEpiC	eye:	n/a
35	chr11:48328132-48328182	AG09309	skin:	n/a
36	chr11:48237358-48237408	HEEpiC	esophagus:	n/a
37	chr11:48285821-48285871	HIPEpiC	eye:	n/a
38	chr11:48191068-48191118	SKMC	muscle:	n/a
39	chr11:48238296-48238346	HRE	kidney:	n/a
40	chr11:48345361-48345411	GM12878	blood:	n/a
41	chr11:48237353-48237403	ProgFib	skin:	n/a
42	chr11:48284249-48284299	GM12878	blood:	n/a
43	chr11:48345815-48345865	AG10803	skin:	n/a
44	chr11:48284249-48284299	H1-hESC	embryonic stem cell:	embryo
45	chr11:48237353-48237403	SAEC	small airway:	n/a
46	chr11:48266856-48266906	SK-N-SH	brain:	n/a
47	chr11:48285200-48285250	HRE	kidney:	n/a
48	chr11:48326388-48326438	AG04449	skin:	fetal
49	chr11:48237358-48237408	HRPEpiC	eye:	n/a
50	chr11:48238724-48238774	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:48194137..48195015-chr11:48231499..48232341,4	MCF-7	breast:
2	chr11:48205381..48206618-chr11:48231139..48232409,4	MCF-7	breast:
3	chr11:48193798..48195313-chr11:48231364..48232253,10	MCF-7	breast:
4	chr11:48292794..48294613-chr11:48297509..48299435,2	K562	blood:
5	chr11:48193798..48195313-chr11:48231364..48232253,10	MCF-7	breast:
6	chr11:48194206..48195039-chr11:49190936..49191807,2	MCF-7	breast:
7	chr11:48234220..48234962-chr11:48329425..48329937,2	MCF-7	breast:
8	chr11:48205861..48206473-chr11:48233802..48234494,2	MCF-7	breast:
9	chr11:48205381..48206618-chr11:48231139..48232409,4	MCF-7	breast:
10	chr11:48205861..48206473-chr11:48233802..48234494,2	MCF-7	breast:
11	chr11:48234220..48234962-chr11:48329425..48329937,2	MCF-7	breast:
12	chr11:48194137..48195015-chr11:48231499..48232341,4	MCF-7	breast:
13	chr11:48292794..48294613-chr11:48297509..48299435,2	K562	blood:

No.	miRNA target gene	miRNA name	Chromosome Location
1	PTPRJ	hsa-miR-124-3p	chr11:48189418-48189438
2	PTPRJ	hsa-miR-328-3p	chr11:48191725-48191748
3	PTPRJ	hsa-miR-155-5p	chr11:48190351-48190373
4	PTPRJ	hsa-miR-124-3p	chr11:48189431-48189437
5	PTPRJ	hsa-miR-16-5p	chr11:48190236-48190242
6	PTPRJ	hsa-miR-16-5p	chr11:48190225-48190243
7	PTPRJ	hsa-miR-155-5p	chr11:48190367-48190373
8	PTPRJ	hsa-miR-26b-5p	chr11:48190233-48190256

Variant related genes	Relation type
OR4X2	TF binding region
OR4B2P	TF binding region
OR4X1	TF binding region
OR4C3	TF binding region
OR4S1	TF binding region
OR4B1	TF binding region
OR4X2	CpG island
OR4B2P	CpG island
OR4X1	CpG island
OR4C3	CpG island
OR4S1	CpG island
OR4B1	CpG island

Extended variants
information (count: 2085 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2085 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11039556	chr11:48188748-48188749	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs540802430	chr11:48188773-48188774	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs369579079	chr11:48188806-48188807	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188934138	chr11:48188844-48188845	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139396147	chr11:48188855-48188856	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs577409423	chr11:48188859-48188860	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs199803858	chr11:48188871-48188872	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs12809012	chr11:48188872-48188873	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs371796701	chr11:48188875-48188876	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs35920791	chr11:48188908-48188909	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs200505007	chr11:48188909-48188910	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs375419721	chr11:48188953-48188954	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs191012650	chr11:48188965-48188966	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529989420	chr11:48188979-48188980	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs73452004	chr11:48188980-48188981	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs542898958	chr11:48189000-48189001	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559529578	chr11:48189026-48189027	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538447514	chr11:48189074-48189075	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs139911163	chr11:48189077-48189078	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs79113573	chr11:48189082-48189083	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568624530	chr11:48189090-48189091	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537835534	chr11:48189149-48189150	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs201256982	chr11:48189171-48189172	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs554299989	chr11:48189178-48189179	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs1058419	chr11:48189182-48189183	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs1058418	chr11:48189202-48189203	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs374139873	chr11:48189218-48189219	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575076305	chr11:48189226-48189227	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534267630	chr11:48189227-48189228	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182290501	chr11:48189372-48189373	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs577468683	chr11:48189413-48189414	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs373842274	chr11:48189449-48189450	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs546441888	chr11:48189474-48189475	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562936929	chr11:48189487-48189488	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs528488829	chr11:48189497-48189498	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs186948486	chr11:48189513-48189514	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs1058417	chr11:48189604-48189605	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7951730	chr11:48189606-48189607	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs1058416	chr11:48189627-48189628	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561979015	chr11:48189686-48189687	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs117902837	chr11:48189911-48189912	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544055903	chr11:48189951-48189952	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs3071027	chr11:48190083-48190084	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs573714428	chr11:48190085-48190086	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs10607467	chr11:48190086-48190087	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs71045551	chr11:48190129-48190130	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs7131268	chr11:48190133-48190134	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs1983072	chr11:48190134-48190135	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs115355320	chr11:48190138-48190139	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs560036006	chr11:48190154-48190155	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Breast cancer	21990379	CNVD
Acute myeloid leukemia	20729466	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD

Chromatin state (count:524 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48131600-48191600	Weak transcription	Small Intestine	intestine
2	chr11:48138200-48192600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr11:48149800-48190600	Weak transcription	Right Ventricle	heart
4	chr11:48151400-48191600	Weak transcription	Stomach Mucosa	stomach
5	chr11:48156400-48191400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr11:48163400-48192400	Weak transcription	Colon Smooth Muscle	Colon
7	chr11:48174000-48190800	Strong transcription	Liver	Liver
8	chr11:48175200-48191200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr11:48175400-48192400	Strong transcription	Primary neutrophils fromperipheralblood	blood
10	chr11:48175600-48191000	Strong transcription	Primary T cells fromperipheralblood	blood
11	chr11:48175800-48190800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr11:48175800-48190800	Weak transcription	HSMMtube	muscle
13	chr11:48175800-48191600	Weak transcription	Rectal Smooth Muscle	rectum
14	chr11:48176000-48190800	Strong transcription	Primary T helper cells fromperipheralblood	blood
15	chr11:48176000-48194600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr11:48176200-48191000	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr11:48176200-48191200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr11:48176200-48192000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr11:48176400-48189000	Strong transcription	Primary T cells from cord blood	blood
20	chr11:48176400-48189200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr11:48176600-48190600	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr11:48176600-48191800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr11:48177000-48190400	Weak transcription	Fetal Muscle Trunk	muscle
24	chr11:48177600-48191000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr11:48177600-48191000	Weak transcription	Fetal Kidney	kidney
26	chr11:48177600-48191200	Strong transcription	Primary B cells from peripheral blood	blood
27	chr11:48177600-48191400	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr11:48178000-48191200	Strong transcription	Primary B cells from cord blood	blood
29	chr11:48178200-48190800	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr11:48179200-48190800	Weak transcription	Left Ventricle	heart
31	chr11:48179200-48193200	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr11:48179400-48191000	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr11:48179400-48192200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr11:48183400-48191000	Strong transcription	Primary T helper cells PMA-I stimulated	--
35	chr11:48184000-48189200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr11:48184000-48189800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr11:48184000-48190000	Strong transcription	Sigmoid Colon	Sigmoid Colon
38	chr11:48184000-48191600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr11:48184200-48190800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr11:48184200-48191000	Strong transcription	Rectal Mucosa Donor 29	rectum
41	chr11:48184400-48190600	Weak transcription	NHLF	lung
42	chr11:48184400-48191200	Weak transcription	Ovary	ovary
43	chr11:48184400-48191200	Weak transcription	HUVEC	blood vessel
44	chr11:48184600-48190600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr11:48184800-48191000	Strong transcription	Placenta	Placenta
46	chr11:48185000-48192000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr11:48185600-48192600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr11:48185800-48188800	Strong transcription	NH-A	brain
49	chr11:48185800-48192400	Weak transcription	Fetal Brain Female	brain
50	chr11:48186000-48190400	Weak transcription	Colonic Mucosa	Colon

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