Variant report

Variant	nsv540928
Chromosome Location	chr11:4628274-4647615
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:594)
CpG islands
(count:733)
Chromatin interactive
region (count:7)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:594 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:4629507-4629808	K562	blood:	n/a	n/a
2	ATF1	chr11:4647476-4647734	K562	blood:	n/a	n/a
3	ATF1	chr11:4640875-4641090	K562	blood:	n/a	n/a
4	BHLHE40	chr11:4629164-4629819	K562	blood:	n/a	chr11:4629490-4629506
5	BRCA1	chr11:4629133-4629295	Hela-S3	cervix:	n/a	n/a
6	CBX3	chr11:4628967-4630004	K562	blood:	n/a	n/a
7	CCNT2	chr11:4629051-4629981	K562	blood:	n/a	chr11:4629061-4629070
8	CEBPB	chr11:4647421-4647749	K562	blood:	n/a	n/a
9	CEBPB	chr11:4647442-4647716	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr11:4641031-4641091	K562	blood:	n/a	n/a
11	CEBPB	chr11:4629219-4629669	Hela-S3	cervix:	n/a	chr11:4629483-4629491 chr11:4629547-4629555
12	CEBPB	chr11:4647363-4647690	MCF-7	breast:	n/a	n/a
13	CHD2	chr11:4629007-4629765	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr11:4629022-4629829	GM12878	blood:	n/a	n/a
15	CHD2	chr11:4628967-4629798	Hela-S3	cervix:	n/a	n/a
16	CHD2	chr11:4629071-4629849	K562	blood:	n/a	n/a
17	CREB1	chr11:4628953-4629773	A549	lung:	n/a	n/a
18	CTCF	chr11:4629120-4629270	SAEC	small airway:	n/a	n/a
19	CTCF	chr11:4647500-4647650	GM12869	blood:	n/a	n/a
20	CTCF	chr11:4647434-4647718	MCF-7	breast:	n/a	n/a
21	CTCF	chr11:4647540-4647690	HepG2	liver:	n/a	n/a
22	CTCF	chr11:4629020-4629170	AG10803	skin:	n/a	n/a
23	CTCF	chr11:4647416-4647838	A549	lung:	n/a	n/a
24	CTCF	chr11:4647560-4647710	GM12868	blood:	n/a	n/a
25	CTCF	chr11:4647540-4647690	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr11:4629340-4629490	AG04449	skin:	n/a	n/a
27	CTCF	chr11:4647463-4647801	HepG2	liver:	n/a	n/a
28	CTCF	chr11:4647540-4647690	HEK293	kidney:	n/a	n/a
29	CTCF	chr11:4647503-4647723	GM13977	blood:	n/a	n/a
30	CTCF	chr11:4647490-4647711	GM19239	blood:	n/a	n/a
31	CTCF	chr11:4647560-4647710	HPAF	blood vessel:	n/a	n/a
32	CTCF	chr11:4647540-4647690	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr11:4647560-4647710	GM12867	blood:	n/a	n/a
34	CTCF	chr11:4647560-4647710	HPF	lung:	n/a	n/a
35	CTCF	chr11:4647444-4647757	Medullo	brain:	n/a	n/a
36	CTCF	chr11:4647490-4647688	GM12892	blood:	n/a	n/a
37	CTCF	chr11:4647540-4647690	GM12865	blood:	n/a	n/a
38	CTCF	chr11:4629460-4629610	AG04449	skin:	n/a	chr11:4629518-4629531 chr11:4629520-4629530
39	CTCF	chr11:4629560-4629710	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr11:4629040-4629190	GM12865	blood:	n/a	n/a
41	CTCF	chr11:4647560-4647710	BJ	skin:	n/a	n/a
42	CTCF	chr11:4647520-4647670	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr11:4647520-4647670	K562	blood:	n/a	n/a
44	CTCF	chr11:4647540-4647690	HAc	cerebellar:	n/a	n/a
45	CTCF	chr11:4647500-4647650	GM12867	blood:	n/a	n/a
46	CTCF	chr11:4647520-4647670	HMEC	breast:	n/a	n/a
47	CTCF	chr11:4647560-4647710	AG09309	skin:	n/a	n/a
48	CTCF	chr11:4647560-4647710	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr11:4647516-4647707	GM10248	blood:	n/a	n/a
50	CTCF	chr11:4647538-4647645	H1-hESC	embryonic stem cell:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4629034-4629084	Hela-S3	cervix:	n/a
2	chr11:4629034-4629084	Hela-S3	cervix:	n/a
3	chr11:4629034-4629084	GM12878	blood:	n/a
4	chr11:4629912-4629962	HCPEpiC	choroid plexus:	n/a
5	chr11:4628823-4628873	GM06990	blood:	n/a
6	chr11:4629606-4629656	AG04449	skin:	fetal
7	chr11:4631906-4631956	HMEC	breast:	n/a
8	chr11:4628823-4628873	HMEC	breast:	n/a
9	chr11:4629432-4629482	AG09319	gingival:	n/a
10	chr11:4629609-4629659	HCT-116	colon:	n/a
11	chr11:4629609-4629659	U87	brain:	n/a
12	chr11:4629749-4629799	AG04450	lung:	fetal
13	chr11:4629912-4629962	NHBE	bronchial:	n/a
14	chr11:4629667-4629717	HUVEC	blood vessel:	n/a
15	chr11:4629609-4629659	NT2-D1	testis:	n/a
16	chr11:4629432-4629482	LNCaP	prostate:	n/a
17	chr11:4631906-4631956	HNPCEpiC	eye:	n/a
18	chr11:4629432-4629482	NHDF-neo	bronchial:	n/a
19	chr11:4629609-4629659	AG10803	skin:	n/a
20	chr11:4629034-4629084	HCF	heart:	n/a
21	chr11:4631906-4631956	HRE	kidney:	n/a
22	chr11:4629667-4629717	T-47D	breast:	n/a
23	chr11:4629357-4629407	ProgFib	skin:	n/a
24	chr11:4629667-4629717	ECC-1	luminal epithelium:	n/a
25	chr11:4629606-4629656	AG09309	skin:	n/a
26	chr11:4631906-4631956	MCF10A-Er-Src	breast:	n/a
27	chr11:4629357-4629407	MCF-7	breast:	n/a
28	chr11:4631906-4631956	MCF-7	breast:	n/a
29	chr11:4629606-4629656	IMR90	lung:	fetal
30	chr11:4629357-4629407	PrEC	prostate:	n/a
31	chr11:4629609-4629659	SAEC	small airway:	n/a
32	chr11:4629667-4629717	MCF10A-Er-Src	breast:	n/a
33	chr11:4629432-4629482	SK-N-SH	brain:	n/a
34	chr11:4629034-4629084	H1-hESC	embryonic stem cell:	embryo
35	chr11:4629597-4629647	AG04450	lung:	fetal
36	chr11:4629432-4629482	NT2-D1	testis:	n/a
37	chr11:4629606-4629656	CMK	blood:	n/a
38	chr11:4629432-4629482	NH-A	brain:	n/a
39	chr11:4629432-4629482	IMR90	lung:	fetal
40	chr11:4629034-4629084	ECC-1	luminal epithelium:	n/a
41	chr11:4629667-4629717	K562	blood:	n/a
42	chr11:4629749-4629799	HCT-116	colon:	n/a
43	chr11:4629597-4629647	HL-60	blood:	n/a
44	chr11:4629597-4629647	IMR90	lung:	fetal
45	chr11:4629667-4629717	HPAEpiC	pulmonary alveolar:	n/a
46	chr11:4629432-4629482	GM12892	blood:	n/a
47	chr11:4629912-4629962	AG04449	skin:	fetal
48	chr11:4628823-4628873	SK-N-SH_RA	brain:	n/a
49	chr11:4629432-4629482	AG04450	lung:	fetal
50	chr11:4629667-4629717	GM12891	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:4208255..4208841-chr11:4647118..4648091,2	K562	blood:
2	chr11:4619365..4621558-chr11:4626252..4629277,3	K562	blood:
3	chr11:4620058..4622735-chr11:4626222..4629091,3	K562	blood:
4	chr11:4625479..4627156-chr11:4627233..4629279,2	K562	blood:
5	chr11:4647527..4648151-chr11:5025801..5026495,2	MCF-7	breast:
6	chr11:4647199..4648030-chr11:5025327..5026179,2	K562	blood:
7	chr11:4626393..4630553-chr11:4632444..4636618,6	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR51D1-1	chr11:4644433-4644768	l_424_chr11:4644432-4650062_testes
2	lnc-OR51D1-1	chr11:4647477-4647663	l_424_chr11:4644432-4650062_testes

No data

Variant related genes	Relation type
TRIM68	TF binding region
TRIM68	CpG island
ENSG00000167333	chromatin interactions
ENSG00000254480	chromatin interactions

Extended variants
information (count: 759 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:759 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547633837	chr11:4628287-4628288	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs149206329	chr11:4628314-4628315	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs112569674	chr11:4628316-4628317	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs537211051	chr11:4628330-4628331	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs182138644	chr11:4628342-4628343	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs576527216	chr11:4628377-4628378	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs534440953	chr11:4628393-4628394	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs552537406	chr11:4628414-4628415	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs574059347	chr11:4628455-4628456	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs541829162	chr11:4628456-4628457	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs563387172	chr11:4628493-4628494	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs185759234	chr11:4628494-4628495	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs575501013	chr11:4628564-4628565	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs545669926	chr11:4628572-4628573	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs564319325	chr11:4628580-4628581	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs532628708	chr11:4628598-4628599	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs547943906	chr11:4628600-4628601	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs116738529	chr11:4628602-4628603	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs530070443	chr11:4628607-4628608	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs143243706	chr11:4628615-4628616	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs570244623	chr11:4628653-4628654	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs537798723	chr11:4628704-4628705	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs552476268	chr11:4628715-4628716	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs138810183	chr11:4628744-4628745	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs375896110	chr11:4628774-4628775	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs57341642	chr11:4628777-4628778	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs534905896	chr11:4628818-4628819	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs190564569	chr11:4628857-4628858	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs1472231	chr11:4628867-4628868	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574195029	chr11:4628886-4628887	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs142066922	chr11:4628920-4628921	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs577619049	chr11:4628960-4628961	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs556954706	chr11:4628978-4628979	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs117924997	chr11:4629002-4629003	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs183008368	chr11:4629012-4629013	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs80035042	chr11:4629021-4629022	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs60367098	chr11:4629041-4629042	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs573039274	chr11:4629051-4629052	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs540432550	chr11:4629074-4629075	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs111779375	chr11:4629075-4629076	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs145681325	chr11:4629085-4629086	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs377367058	chr11:4629120-4629121	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs114200010	chr11:4629134-4629135	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs11033009	chr11:4629140-4629141	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs531098095	chr11:4629152-4629153	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs552421059	chr11:4629156-4629157	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs115807560	chr11:4629168-4629169	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs185387310	chr11:4629177-4629178	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs531655279	chr11:4629187-4629188	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs546796730	chr11:4629203-4629204	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Esophageal adenocarcinoma	18519675	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:537 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4618600-4628400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr11:4619400-4628800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr11:4620600-4628400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr11:4622600-4628600	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr11:4623000-4628400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr11:4623400-4628400	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr11:4623400-4628400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr11:4623800-4628400	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr11:4624200-4628600	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr11:4626400-4628400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr11:4626600-4628400	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr11:4626600-4628400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr11:4626600-4629000	Weak transcription	Gastric	stomach
14	chr11:4626800-4628400	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr11:4626800-4628600	Weak transcription	Fetal Muscle Trunk	muscle
16	chr11:4626800-4629000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr11:4626800-4629000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr11:4627000-4628400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr11:4627400-4628400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr11:4627400-4628800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr11:4627600-4628400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr11:4627600-4628400	Enhancers	Fetal Intestine Large	intestine
23	chr11:4627600-4628400	Enhancers	HMEC	breast
24	chr11:4627600-4629000	Flanking Active TSS	Primary hematopoietic stem cells	blood
25	chr11:4627600-4629000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr11:4627800-4628400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr11:4627800-4628400	Enhancers	Fetal Brain Female	brain
28	chr11:4627800-4628400	Enhancers	Fetal Stomach	stomach
29	chr11:4627800-4628400	Enhancers	Fetal Thymus	thymus
30	chr11:4627800-4628600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr11:4627800-4628600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
32	chr11:4627800-4628800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr11:4627800-4628800	Flanking Active TSS	Duodenum Mucosa	Duodenum
34	chr11:4627800-4628800	Flanking Active TSS	Dnd41	blood
35	chr11:4627800-4629000	Flanking Active TSS	Primary T cells from cord blood	blood
36	chr11:4627800-4629000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr11:4627800-4629000	Enhancers	Spleen	Spleen
38	chr11:4627800-4629000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
39	chr11:4627800-4629400	Active TSS	Sigmoid Colon	Sigmoid Colon
40	chr11:4628000-4628400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr11:4628000-4628400	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr11:4628000-4628400	Enhancers	Primary B cells from cord blood	blood
43	chr11:4628000-4628400	Enhancers	Primary T cells fromperipheralblood	blood
44	chr11:4628000-4628400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr11:4628000-4628400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr11:4628000-4628400	Enhancers	Pancreas	Pancrea
47	chr11:4628000-4628400	Enhancers	Small Intestine	intestine
48	chr11:4628000-4628400	Enhancers	NHEK	skin
49	chr11:4628000-4628600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr11:4628000-4628600	Enhancers	Cortex derived primary cultured neurospheres	brain

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