Variant report

Variant	nsv553371
Chromosome Location	chr11:6395690-6434465
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1014)
CpG islands
(count:1040)
Chromatin interactive
region (count:66)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1014 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:6400542-6400802	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:6400552-6400815	K562	blood:	n/a	n/a
3	ATF1	chr11:6411274-6411813	K562	blood:	n/a	n/a
4	ATF2	chr11:6411170-6411697	GM12878	blood:	n/a	n/a
5	ATF2	chr11:6423784-6424277	GM12878	blood:	n/a	n/a
6	ATF2	chr11:6410889-6411874	GM12878	blood:	n/a	n/a
7	ATF2	chr11:6423650-6424338	GM12878	blood:	n/a	n/a
8	BACH1	chr11:6406483-6406508	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr11:6411154-6411494	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr11:6411086-6411773	GM12878	blood:	n/a	n/a
11	BATF	chr11:6423743-6424226	GM12878	blood:	n/a	chr11:6423989-6423999 chr11:6423988-6423999
12	BATF	chr11:6423868-6424182	GM12878	blood:	n/a	chr11:6423989-6423999 chr11:6423988-6423999
13	BCL11A	chr11:6423880-6424254	GM12878	blood:	n/a	n/a
14	BCL3	chr11:6423800-6424276	GM12878	blood:	n/a	n/a
15	BCL3	chr11:6411056-6411871	GM12878	blood:	n/a	chr11:6411671-6411680
16	BCL3	chr11:6411281-6411705	GM12878	blood:	n/a	chr11:6411671-6411680
17	BCLAF1	chr11:6411148-6411880	GM12878	blood:	n/a	chr11:6411671-6411680
18	BCLAF1	chr11:6400426-6400832	GM12878	blood:	n/a	n/a
19	BCLAF1	chr11:6410995-6412067	GM12878	blood:	n/a	chr11:6411671-6411680
20	BCLAF1	chr11:6423682-6424317	GM12878	blood:	n/a	n/a
21	BHLHE40	chr11:6399596-6399787	GM12878	blood:	n/a	n/a
22	BHLHE40	chr11:6410624-6410850	K562	blood:	n/a	n/a
23	BHLHE40	chr11:6411212-6411676	A549	lung:	n/a	n/a
24	BHLHE40	chr11:6411142-6411867	HepG2	liver:	n/a	n/a
25	BHLHE40	chr11:6400505-6400701	K562	blood:	n/a	n/a
26	BHLHE40	chr11:6423407-6423747	HepG2	liver:	n/a	chr11:6423583-6423604
27	BHLHE40	chr11:6423402-6424231	GM12878	blood:	n/a	chr11:6423583-6423604
28	BHLHE40	chr11:6399598-6400003	K562	blood:	n/a	chr11:6399804-6399813 chr11:6399803-6399812 chr11:6399797-6399818 chr11:6399801-6399814 chr11:6399802-6399811 chr11:6399803-6399812
29	BHLHE40	chr11:6399632-6399947	HepG2	liver:	n/a	chr11:6399804-6399813 chr11:6399803-6399812 chr11:6399797-6399818 chr11:6399801-6399814 chr11:6399802-6399811 chr11:6399803-6399812
30	BHLHE40	chr11:6410767-6411928	GM12878	blood:	n/a	n/a
31	BHLHE40	chr11:6423491-6423716	K562	blood:	n/a	chr11:6423583-6423604
32	BHLHE40	chr11:6411106-6411924	K562	blood:	n/a	n/a
33	BRCA1	chr11:6411305-6411832	GM12878	blood:	n/a	n/a
34	BRCA1	chr11:6409010-6409188	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr11:6411493-6411577	H1-hESC	embryonic stem cell:	n/a	n/a
36	BRCA1	chr11:6411159-6411754	Hela-S3	cervix:	n/a	n/a
37	CBX3	chr11:6411077-6411771	K562	blood:	n/a	n/a
38	CCNT2	chr11:6411105-6412040	K562	blood:	n/a	chr11:6411592-6411601 chr11:6411514-6411523
39	CEBPB	chr11:6398306-6398536	A549	lung:	n/a	chr11:6398397-6398408
40	CEBPB	chr11:6398295-6398503	HepG2	liver:	n/a	chr11:6398397-6398408
41	CEBPB	chr11:6409280-6409596	K562	blood:	n/a	chr11:6409301-6409312
42	CEBPB	chr11:6409184-6409573	MCF-7	breast:	n/a	chr11:6409301-6409312
43	CEBPB	chr11:6399565-6399789	K562	blood:	n/a	chr11:6399674-6399685
44	CEBPB	chr11:6409345-6409565	HepG2	liver:	n/a	n/a
45	CEBPB	chr11:6409143-6409596	HepG2	liver:	n/a	chr11:6409301-6409312
46	CEBPB	chr11:6412500-6412558	IMR90	lung:	n/a	n/a
47	CEBPB	chr11:6411220-6411282	K562	blood:	n/a	n/a
48	CEBPB	chr11:6409160-6409607	MCF-7	breast:	n/a	chr11:6409301-6409312
49	CEBPB	chr11:6409040-6409756	A549	lung:	n/a	chr11:6409301-6409312
50	CEBPB	chr11:6402026-6402136	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:6416634-6416684	AG09309	skin:	n/a
2	chr11:6418966-6419016	HAEpiC	amniotic membrane:	n/a
3	chr11:6411615-6411665	AG04449	skin:	fetal
4	chr11:6416634-6416684	AG09309	skin:	n/a
5	chr11:6418966-6419016	HAEpiC	amniotic membrane:	n/a
6	chr11:6411615-6411665	AG04449	skin:	fetal
7	chr11:6411382-6411432	CMK	blood:	n/a
8	chr11:6411469-6411519	HEK293	kidney:	embryo
9	chr11:6411382-6411432	GM12891	blood:	n/a
10	chr11:6425978-6426028	HEK293	kidney:	embryo
11	chr11:6412852-6412902	AG10803	skin:	n/a
12	chr11:6408135-6408185	U87	brain:	n/a
13	chr11:6418966-6419016	HCM	heart:	n/a
14	chr11:6411382-6411432	GM19239	blood:	n/a
15	chr11:6401965-6402015	Caco-2	colon:	n/a
16	chr11:6413036-6413086	PrEC	prostate:	n/a
17	chr11:6411469-6411519	T-47D	breast:	n/a
18	chr11:6412852-6412902	CMK	blood:	n/a
19	chr11:6408135-6408185	HIPEpiC	eye:	n/a
20	chr11:6411087-6411137	GM19239	blood:	n/a
21	chr11:6411382-6411432	GM12892	blood:	n/a
22	chr11:6411486-6411536	AG04450	lung:	fetal
23	chr11:6401965-6402015	HNPCEpiC	eye:	n/a
24	chr11:6411615-6411665	Hepatocyte	liver:	n/a
25	chr11:6425978-6426028	NHDF-neo	bronchial:	n/a
26	chr11:6412852-6412902	H1-hESC	embryonic stem cell:	embryo
27	chr11:6411824-6411874	BJ	skin:	n/a
28	chr11:6415462-6415512	HEK293	kidney:	embryo
29	chr11:6415462-6415512	AG09319	gingival:	n/a
30	chr11:6418966-6419016	SKMC	muscle:	n/a
31	chr11:6415462-6415512	CMK	blood:	n/a
32	chr11:6415462-6415512	ProgFib	skin:	n/a
33	chr11:6411396-6411446	HL-60	blood:	n/a
34	chr11:6411087-6411137	HCPEpiC	choroid plexus:	n/a
35	chr11:6413036-6413086	HAEpiC	amniotic membrane:	n/a
36	chr11:6411394-6411444	HMEC	breast:	n/a
37	chr11:6411394-6411444	AG04449	skin:	fetal
38	chr11:6401965-6402015	PrEC	prostate:	n/a
39	chr11:6411396-6411446	Hela-S3	cervix:	n/a
40	chr11:6401965-6402015	Hepatocyte	liver:	n/a
41	chr11:6411382-6411432	AG09319	gingival:	n/a
42	chr11:6413036-6413086	NHDF-neo	bronchial:	n/a
43	chr11:6413036-6413086	K562	blood:	n/a
44	chr11:6425978-6426028	AG04450	lung:	fetal
45	chr11:6418966-6419016	NHDF-neo	bronchial:	n/a
46	chr11:6416634-6416684	HL-60	blood:	n/a
47	chr11:6411486-6411536	AoSMC	blood vessel:	n/a
48	chr11:6411824-6411874	GM12878	blood:	n/a
49	chr11:6415462-6415512	HUVEC	blood vessel:	n/a
50	chr11:6411396-6411446	AG04449	skin:	fetal

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:6391164..6393393-chr11:6398964..6400664,2	K562	blood:
2	chr11:6411376..6413453-chr11:6431769..6433679,2	MCF-7	breast:
3	chr11:6400114..6400745-chr11:6552411..6553083,2	K562	blood:
4	chr11:6411491..6417099-chr11:6417551..6421246,9	K562	blood:
5	chr11:6429931..6435317-chr11:6436450..6440768,9	K562	blood:
6	chr11:6408399..6412955-chr11:6499739..6504366,6	K562	blood:
7	chr11:6423909..6425899-chr11:6427408..6428940,2	K562	blood:
8	chr11:6399574..6400171-chr11:6459933..6460483,2	K562	blood:
9	chr11:6411247..6414298-chr11:6438390..6440543,3	K562	blood:
10	chr11:6418257..6421798-chr11:6425467..6428210,3	K562	blood:
11	chr11:6414850..6417126-chr11:6418576..6421791,3	K562	blood:
12	chr11:6414850..6417126-chr11:6418576..6421791,3	K562	blood:
13	chr11:6400252..6401140-chr11:6704657..6705206,2	MCF-7	breast:
14	chr11:6409945..6411643-chr11:6415896..6417521,2	K562	blood:
15	chr11:6414472..6417061-chr11:6417337..6420893,4	MCF-7	breast:
16	chr11:6417472..6422736-chr11:6426508..6430441,6	K562	blood:
17	chr11:6400196..6400930-chr11:6526550..6527549,3	K562	blood:
18	chr11:6416395..6419140-chr11:6421836..6424422,2	K562	blood:
19	chr11:6408886..6411627-chr11:6701722..6704947,4	MCF-7	breast:
20	chr11:6398312..6400551-chr11:6465206..6467299,2	K562	blood:
21	chr11:6431700..6434113-chr11:6463809..6466490,2	K562	blood:
22	chr11:6419635..6421208-chr11:6500861..6503697,2	K562	blood:
23	chr11:6400044..6400715-chr11:6726460..6727367,2	K562	blood:
24	chr11:6398714..6402192-chr11:6493478..6496580,5	K562	blood:
25	chr11:6417472..6422736-chr11:6426508..6430441,6	K562	blood:
26	chr11:6410112..6413030-chr11:6499663..6503082,4	K562	blood:
27	chr11:6408446..6411520-chr11:6632512..6635216,4	K562	blood:
28	chr11:6427745..6429783-chr11:6431665..6434333,2	MCF-7	breast:
29	chr11:6389874..6394705-chr11:6397417..6400664,4	K562	blood:
30	chr11:6413402..6415677-chr11:6493747..6495286,2	K562	blood:
31	chr11:6399284..6401140-chr11:6688661..6690633,2	MCF-7	breast:
32	chr11:6399787..6402343-chr11:6476528..6478169,2	MCF-7	breast:
33	chr11:6397566..6399212-chr11:6439542..6442003,2	K562	blood:
34	chr11:6427745..6429783-chr11:6431665..6434333,2	MCF-7	breast:
35	chr11:6411642..6413741-chr11:6439069..6440811,2	K562	blood:
36	chr11:6424083..6426944-chr11:6501315..6502949,2	K562	blood:
37	chr11:6408815..6414157-chr11:6415408..6420403,9	K562	blood:
38	chr11:6416395..6419140-chr11:6421836..6424422,2	K562	blood:
39	chr11:6404689..6406425-chr11:6499967..6502513,2	MCF-7	breast:
40	chr11:6424151..6426717-chr11:6432076..6433999,2	K562	blood:
41	chr11:6434429..6436954-chr11:6440201..6441925,2	K562	blood:
42	chr11:6427378..6429744-chr11:6430680..6434211,4	K562	blood:
43	chr11:6409955..6412390-chr11:6502445..6504607,2	MCF-7	breast:
44	chr11:6410391..6413968-chr11:6413984..6416522,3	MCF-7	breast:
45	chr11:6408815..6414157-chr11:6415408..6420403,9	K562	blood:
46	chr11:6400453..6402201-chr11:6403811..6406719,2	K562	blood:
47	chr11:6402446..6404260-chr11:6499323..6501427,2	K562	blood:
48	chr11:6409945..6411643-chr11:6415896..6417521,2	K562	blood:
49	chr11:6427378..6429744-chr11:6430680..6434211,4	K562	blood:
50	chr11:6398714..6402788-chr11:6492263..6496580,6	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FXC1-2	chr11:6413236-6413286	NONHSAT017714
2	lnc-FXC1-2	chr11:6411670-6412043	NONHSAT017714

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	APBB1	hsa-miR-148b-3p	chr11:6423415-6423438
2	APBB1	hsa-miR-148b-3p	chr11:6416355-6416374

Variant related genes	Relation type
SMPD1	TF binding region
APBB1	TF binding region
SMPD1	CpG island
APBB1	CpG island
ENSG00000110171	chromatin interactions
ENSG00000265264	chromatin interactions
ENSG00000110169	chromatin interactions
ENSG00000166313	chromatin interactions
ENSG00000158042	chromatin interactions
ENSG00000166311	chromatin interactions
ENSG00000132286	chromatin interactions
ENSG00000166337	chromatin interactions
ENSG00000132254	chromatin interactions

Extended variants
information (count: 1774 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1774 , 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	rs2682086	chr11:6395690-6395691	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs75392765	chr11:6395718-6395719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs575245118	chr11:6395746-6395747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556843894	chr11:6395758-6395759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs532686814	chr11:6395794-6395795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2682087	chr11:6395795-6395796	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs114378757	chr11:6395798-6395799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188048980	chr11:6395799-6395800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192857649	chr11:6395803-6395804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569898819	chr11:6395842-6395843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537330978	chr11:6395851-6395852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs7926099	chr11:6395855-6395856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558506206	chr11:6395867-6395868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2723673	chr11:6396007-6396008	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs554647819	chr11:6396014-6396015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540801439	chr11:6396029-6396030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552657011	chr11:6396053-6396054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11351301	chr11:6396081-6396082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574157798	chr11:6396092-6396093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541499448	chr11:6396094-6396095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150712357	chr11:6396106-6396107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs115375131	chr11:6396179-6396180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531937223	chr11:6396192-6396193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532087391	chr11:6396281-6396282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544076543	chr11:6396358-6396359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565542195	chr11:6396379-6396380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs72896243	chr11:6396421-6396422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547964052	chr11:6396447-6396448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566187423	chr11:6396497-6396498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573219118	chr11:6396505-6396506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537600404	chr11:6396518-6396519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530207615	chr11:6396519-6396520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs377010269	chr11:6396531-6396532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545742959	chr11:6396541-6396542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7937560	chr11:6396546-6396547	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs2723674	chr11:6396547-6396548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs386750271	chr11:6396554-6396555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570369469	chr11:6396555-6396556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534521641	chr11:6396556-6396557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7936698	chr11:6396563-6396564	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs574236905	chr11:6396572-6396573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2723675	chr11:6396573-6396574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186640580	chr11:6396576-6396577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs1809641	chr11:6396587-6396588	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs10839558	chr11:6396607-6396608	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs191402269	chr11:6396616-6396617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533875535	chr11:6396624-6396625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs11370603	chr11:6396625-6396626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs397747987	chr11:6396630-6396631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374933072	chr11:6396636-6396637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1793 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:6384600-6399800	Weak transcription	Right Atrium	heart
2	chr11:6393200-6397000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr11:6393400-6401400	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr11:6393400-6401600	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr11:6393400-6401800	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr11:6393600-6396600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr11:6393600-6397000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr11:6397000-6397200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr11:6397000-6397400	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr11:6397000-6397400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr11:6397000-6397800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr11:6397200-6397400	Enhancers	H9 Cell Line	embryonic stem cell
13	chr11:6397200-6397400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:6397200-6397800	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr11:6397400-6397800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr11:6397400-6399200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr11:6397400-6401200	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr11:6397400-6401600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr11:6397400-6401800	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr11:6397600-6397800	Enhancers	Primary T cells from cord blood	blood
21	chr11:6397600-6397800	Enhancers	Primary T cells fromperipheralblood	blood
22	chr11:6397600-6397800	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr11:6397600-6397800	Enhancers	Primary T helper cells fromperipheralblood	blood
24	chr11:6397600-6397800	Enhancers	Adipose Nuclei	Adipose
25	chr11:6397600-6399200	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr11:6397800-6398800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr11:6397800-6399000	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr11:6397800-6399200	Weak transcription	Adipose Nuclei	Adipose
29	chr11:6397800-6401800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr11:6398000-6399000	Weak transcription	Primary T cells from cord blood	blood
31	chr11:6398000-6399000	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr11:6398000-6399000	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr11:6398800-6399000	Enhancers	HUVEC	blood vessel
34	chr11:6398800-6399400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr11:6399000-6399200	Enhancers	Primary T cells from cord blood	blood
36	chr11:6399000-6399200	Enhancers	Primary T helper naive cells from peripheral blood	blood
37	chr11:6399000-6399200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr11:6399000-6399200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr11:6399000-6399400	Enhancers	Primary B cells from cord blood	blood
40	chr11:6399000-6399400	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr11:6399000-6399600	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr11:6399000-6400200	Enhancers	Primary T cells fromperipheralblood	blood
43	chr11:6399000-6400400	Enhancers	Fetal Thymus	thymus
44	chr11:6399000-6400400	Flanking Active TSS	HUVEC	blood vessel
45	chr11:6399000-6400600	Enhancers	Primary B cells from peripheral blood	blood
46	chr11:6399000-6400600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr11:6399000-6400600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr11:6399000-6400600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr11:6399000-6401200	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr11:6399000-6402000	Enhancers	Primary T helper cells PMA-I stimulated	--

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