Variant report

Variant	esv3322713
Chromosome Location	chr11:6423376-6427874
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	ATF2	chr11:6423784-6424277	GM12878	blood:	n/a	n/a
2	ATF2	chr11:6423650-6424338	GM12878	blood:	n/a	n/a
3	BATF	chr11:6423868-6424182	GM12878	blood:	n/a	chr11:6423989-6423999 chr11:6423988-6423999
4	BATF	chr11:6423743-6424226	GM12878	blood:	n/a	chr11:6423989-6423999 chr11:6423988-6423999
5	BCL11A	chr11:6423880-6424254	GM12878	blood:	n/a	n/a
6	BCL3	chr11:6423800-6424276	GM12878	blood:	n/a	n/a
7	BCLAF1	chr11:6423682-6424317	GM12878	blood:	n/a	n/a
8	BHLHE40	chr11:6423402-6424231	GM12878	blood:	n/a	chr11:6423583-6423604
9	BHLHE40	chr11:6423491-6423716	K562	blood:	n/a	chr11:6423583-6423604
10	BHLHE40	chr11:6423407-6423747	HepG2	liver:	n/a	chr11:6423583-6423604
11	CEBPB	chr11:6426462-6426908	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr11:6423666-6424378	GM12878	blood:	n/a	n/a
13	CHD1	chr11:6423970-6424105	GM12878	blood:	n/a	n/a
14	CHD2	chr11:6423529-6424293	GM12878	blood:	n/a	n/a
15	CREB1	chr11:6426514-6426963	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr11:6423955-6423977	Spleen_OC	spleen:	n/a	n/a
17	CTCF	chr11:6427640-6427790	Caco-2	colon:	n/a	n/a
18	CTCF	chr11:6426555-6426580	Lung_OC	lung:	n/a	n/a
19	CTCF	chr11:6424920-6425070	A549	lung:	n/a	n/a
20	CTCF	chr11:6423700-6423850	GM12873	blood:	n/a	n/a
21	CTCF	chr11:6423996-6424076	GM12878	blood:	n/a	n/a
22	CTCF	chr11:6423479-6423521	GM19239	blood:	n/a	n/a
23	CTCF	chr11:6423979-6423989	Spleen_OC	spleen:	n/a	n/a
24	EBF1	chr11:6423745-6424203	GM12878	blood:	n/a	n/a
25	EBF1	chr11:6423847-6424233	GM12878	blood:	n/a	n/a
26	ELK1	chr11:6423943-6424142	GM12878	blood:	n/a	n/a
27	EP300	chr11:6426420-6426936	H1-hESC	embryonic stem cell:	n/a	n/a
28	EP300	chr11:6423914-6424174	GM12878	blood:	n/a	n/a
29	EP300	chr11:6423453-6423622	HepG2	liver:	n/a	n/a
30	EP300	chr11:6423690-6424278	GM12878	blood:	n/a	n/a
31	EP300	chr11:6423605-6424275	GM12878	blood:	n/a	n/a
32	ETS1	chr11:6423817-6424360	GM12878	blood:	n/a	n/a
33	ETS1	chr11:6423773-6424277	GM12878	blood:	n/a	n/a
34	FOXM1	chr11:6423627-6424409	GM12878	blood:	n/a	n/a
35	FOXM1	chr11:6423724-6424326	GM12878	blood:	n/a	n/a
36	GABPA	chr11:6423948-6424399	HL-60	blood:	n/a	n/a
37	GABPA	chr11:6423880-6424204	GM12878	blood:	n/a	n/a
38	GABPA	chr11:6423995-6424192	GM12878	blood:	n/a	n/a
39	HNF4A	chr11:6423331-6423641	HepG2	liver:	n/a	chr11:6423488-6423503 chr11:6423490-6423502 chr11:6423489-6423503 chr11:6423485-6423507
40	HNF4A	chr11:6423362-6423627	HepG2	liver:	n/a	chr11:6423488-6423503 chr11:6423490-6423502 chr11:6423489-6423503 chr11:6423485-6423507
41	IKZF1	chr11:6423806-6424303	GM12878	blood:	n/a	n/a
42	IRF4	chr11:6423798-6424307	GM12878	blood:	n/a	n/a
43	IRF4	chr11:6423791-6424289	GM12878	blood:	n/a	n/a
44	JUND	chr11:6426215-6426392	H1-hESC	embryonic stem cell:	n/a	n/a
45	MAX	chr11:6423509-6423737	HepG2	liver:	n/a	chr11:6423587-6423600 chr11:6423589-6423598 chr11:6423589-6423598 chr11:6423587-6423600
46	MAX	chr11:6425132-6425937	NB4	blood:	n/a	chr11:6425636-6425646
47	MAX	chr11:6423502-6424218	NB4	blood:	n/a	chr11:6423587-6423600 chr11:6423589-6423598 chr11:6423589-6423598 chr11:6423587-6423600
48	MAX	chr11:6423401-6424256	GM12878	blood:	n/a	chr11:6423587-6423600 chr11:6423589-6423598 chr11:6423589-6423598 chr11:6423587-6423600
49	MAX	chr11:6426554-6426875	H1-hESC	embryonic stem cell:	n/a	n/a
50	MAZ	chr11:6423559-6424350	GM12878	blood:	n/a	chr11:6423587-6423600 chr11:6423589-6423598 chr11:6423589-6423598 chr11:6423587-6423600

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:6425978-6426028	HRCEpiC	kidney:	n/a
2	chr11:6425978-6426028	Hepatocyte	liver:	n/a
3	chr11:6425978-6426028	HEEpiC	esophagus:	n/a
4	chr11:6425978-6426028	ProgFib	skin:	n/a
5	chr11:6425978-6426028	HepG2	liver:	n/a
6	chr11:6425978-6426028	K562	blood:	n/a
7	chr11:6425978-6426028	AoSMC	blood vessel:	n/a
8	chr11:6425978-6426028	PANC-1	pancreas:	n/a
9	chr11:6425978-6426028	U87	brain:	n/a
10	chr11:6425978-6426028	Hela-S3	cervix:	n/a
11	chr11:6425978-6426028	HCPEpiC	choroid plexus:	n/a
12	chr11:6425978-6426028	HNPCEpiC	eye:	n/a
13	chr11:6425978-6426028	HIPEpiC	eye:	n/a
14	chr11:6425978-6426028	HCF	heart:	n/a
15	chr11:6425978-6426028	BJ	skin:	n/a
16	chr11:6425978-6426028	HCM	heart:	n/a
17	chr11:6425978-6426028	GM06990	blood:	n/a
18	chr11:6425978-6426028	HRPEpiC	eye:	n/a
19	chr11:6425978-6426028	HCT-116	colon:	n/a
20	chr11:6425978-6426028	Jurkat	blood:	n/a
21	chr11:6425978-6426028	HMEC	breast:	n/a
22	chr11:6425978-6426028	PFSK-1	brain:	n/a
23	chr11:6425978-6426028	MCF-7	breast:	n/a
24	chr11:6425978-6426028	GM12892	blood:	n/a
25	chr11:6425978-6426028	GM12878	blood:	n/a
26	chr11:6425978-6426028	GM12891	blood:	n/a
27	chr11:6425978-6426028	HRE	kidney:	n/a
28	chr11:6425978-6426028	NT2-D1	testis:	n/a
29	chr11:6425978-6426028	CMK	blood:	n/a
30	chr11:6425978-6426028	PrEC	prostate:	n/a
31	chr11:6425978-6426028	RPTEC	kidney:	n/a
32	chr11:6425978-6426028	HPAEpiC	pulmonary alveolar:	n/a
33	chr11:6425978-6426028	HAEpiC	amniotic membrane:	n/a
34	chr11:6425978-6426028	A549	lung:	n/a
35	chr11:6425978-6426028	MCF10A-Er-Src	breast:	n/a
36	chr11:6425978-6426028	BE2_C	brain:	n/a
37	chr11:6425978-6426028	NHBE	bronchial:	n/a
38	chr11:6425978-6426028	GM19239	blood:	n/a
39	chr11:6425978-6426028	NH-A	brain:	n/a
40	chr11:6425978-6426028	SK-N-SH	brain:	n/a
41	chr11:6425978-6426028	HEK293	kidney:	embryo
42	chr11:6425978-6426028	SKMC	muscle:	n/a
43	chr11:6425978-6426028	ovcar-3	ovarian:	n/a
44	chr11:6425978-6426028	LNCaP	prostate:	n/a
45	chr11:6425978-6426028	SK-N-MC	brain:	n/a
46	chr11:6425978-6426028	SAEC	small airway:	n/a
47	chr11:6425978-6426028	AG09309	skin:	n/a
48	chr11:6425978-6426028	IMR90	lung:	fetal
49	chr11:6425978-6426028	NB4	blood:	n/a
50	chr11:6425978-6426028	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:6417472..6422736-chr11:6426508..6430441,6	K562	blood:
2	chr11:6423909..6425899-chr11:6427408..6428940,2	K562	blood:
3	chr11:6424462..6426944-chr11:6501449..6504348,2	K562	blood:
4	chr11:6423909..6426033-chr11:6427408..6429130,2	K562	blood:
5	chr11:6427745..6429783-chr11:6431665..6434333,2	MCF-7	breast:
6	chr11:6424083..6426944-chr11:6501315..6502949,2	K562	blood:
7	chr11:6427378..6429744-chr11:6430680..6434211,4	K562	blood:
8	chr11:6416395..6419140-chr11:6421836..6424422,2	K562	blood:

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

Variant related genes	Relation type
APBB1	TF binding region
APBB1	CpG island
ENSG00000166313	chromatin interactions
ENSG00000132254	chromatin interactions
ENSG00000265264	chromatin interactions
ENSG00000132286	chromatin interactions

Extended variants
information (count: 206 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:206 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371138376	chr11:6423381-6423382	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs145282654	chr11:6423419-6423420	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region miRNA target site	2 gene(s)	Overlapped CNVs	n/a
3	rs376117819	chr11:6423420-6423421	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region miRNA target site	2 gene(s)	Overlapped CNVs	n/a
4	rs566748642	chr11:6423458-6423459	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs200798949	chr11:6423468-6423469	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs77140502	chr11:6423471-6423472	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs112050857	chr11:6423472-6423473	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs567409959	chr11:6423491-6423492	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs544653093	chr11:6423537-6423538	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs373658938	chr11:6423538-6423539	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs368152799	chr11:6423541-6423542	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs555807584	chr11:6423559-6423560	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs577254190	chr11:6423562-6423563	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs138430111	chr11:6423563-6423564	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs555184220	chr11:6423588-6423589	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs2075583	chr11:6423630-6423631	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs573449336	chr11:6423650-6423651	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs540880380	chr11:6423655-6423656	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs562145134	chr11:6423690-6423691	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs76704657	chr11:6423746-6423747	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs544732602	chr11:6423790-6423791	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs562953394	chr11:6423791-6423792	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs201889999	chr11:6423826-6423827	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs370357442	chr11:6423864-6423865	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs1800425	chr11:6423873-6423874	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs200624007	chr11:6423886-6423887	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs373773932	chr11:6423895-6423896	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs371684331	chr11:6423905-6423906	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs1800424	chr11:6423907-6423908	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs143740206	chr11:6423941-6423942	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs375733189	chr11:6423942-6423943	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs368805217	chr11:6423943-6423944	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs371824310	chr11:6423946-6423947	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs148143455	chr11:6423947-6423948	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs144059856	chr11:6423949-6423950	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs369323672	chr11:6423971-6423972	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs202061326	chr11:6423973-6423974	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs374765383	chr11:6423993-6423994	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs538030062	chr11:6424042-6424043	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs547078475	chr11:6424076-6424077	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs549495400	chr11:6424083-6424084	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs569161573	chr11:6424125-6424126	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs538288000	chr11:6424128-6424129	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs73398870	chr11:6424142-6424143	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs571960240	chr11:6424170-6424171	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs534245939	chr11:6424173-6424174	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs555990888	chr11:6424203-6424204	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs114619614	chr11:6424238-6424239	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs544796071	chr11:6424258-6424259	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs563014386	chr11:6424261-6424262	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	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:370 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:6412400-6425600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr11:6412600-6426000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr11:6412600-6427000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr11:6412800-6425600	Weak transcription	Fetal Kidney	kidney
5	chr11:6412800-6426200	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr11:6412800-6439400	Weak transcription	HUVEC	blood vessel
7	chr11:6413000-6425200	Weak transcription	Duodenum Mucosa	Duodenum
8	chr11:6413400-6425400	Strong transcription	Fetal Muscle Leg	muscle
9	chr11:6413400-6425600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr11:6413400-6439200	Weak transcription	Psoas Muscle	Psoas
11	chr11:6414200-6426200	Strong transcription	Fetal Intestine Small	intestine
12	chr11:6414600-6425600	Strong transcription	Cortex derived primary cultured neurospheres	brain
13	chr11:6414800-6424200	Strong transcription	Fetal Brain Female	brain
14	chr11:6414800-6425400	Genic enhancers	Brain Cingulate Gyrus	brain
15	chr11:6414800-6434000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr11:6415200-6425400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr11:6415600-6423400	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr11:6415800-6427000	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr11:6416000-6423800	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr11:6416400-6439400	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr11:6416400-6440000	Weak transcription	Liver	Liver
22	chr11:6416600-6426400	Weak transcription	Colonic Mucosa	Colon
23	chr11:6417800-6425600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr11:6418200-6424400	Genic enhancers	Brain Substantia Nigra	brain
25	chr11:6418800-6425000	Strong transcription	Aorta	Aorta
26	chr11:6419400-6423800	Weak transcription	NH-A	brain
27	chr11:6419400-6425400	Strong transcription	Brain Germinal Matrix	brain
28	chr11:6419400-6435200	Weak transcription	Fetal Heart	heart
29	chr11:6419400-6439400	Weak transcription	Rectal Smooth Muscle	rectum
30	chr11:6419600-6425200	Strong transcription	Fetal Intestine Large	intestine
31	chr11:6419600-6425400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr11:6419600-6425600	Strong transcription	Stomach Smooth Muscle	stomach
33	chr11:6419600-6439400	Weak transcription	Osteobl	bone
34	chr11:6419800-6424800	Strong transcription	Fetal Lung	lung
35	chr11:6419800-6425600	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr11:6419800-6425800	Strong transcription	Fetal Stomach	stomach
37	chr11:6420000-6423600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr11:6420000-6424200	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr11:6420000-6425000	Strong transcription	Lung	lung
40	chr11:6420000-6425600	Weak transcription	NHDF-Ad	bronchial
41	chr11:6420200-6424000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr11:6420400-6423400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr11:6420400-6425600	Strong transcription	Duodenum Smooth Muscle	Duodenum
44	chr11:6420600-6423400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr11:6420600-6425400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr11:6420600-6431200	Weak transcription	Ovary	ovary
47	chr11:6420800-6424200	Weak transcription	Fetal Brain Male	brain
48	chr11:6420800-6425400	Strong transcription	NHLF	lung
49	chr11:6420800-6426000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr11:6420800-6426600	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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