Variant report

Variant	esv3440608
Chromosome Location	chr11:47379026-47381524
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:59)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:59 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr11:47377019-47379137	GM12878	blood:	n/a	chr11:47377212-47377225
2	BCL3	chr11:47379522-47380304	GM12878	blood:	n/a	n/a
3	BCL3	chr11:47377142-47379210	GM12878	blood:	n/a	chr11:47377212-47377225
4	BCL3	chr11:47379439-47380264	GM12878	blood:	n/a	n/a
5	CTCF	chr11:47381380-47381530	HL-60	blood:	n/a	n/a
6	CTCF	chr11:47380264-47380295	GM19239	blood:	n/a	n/a
7	CTCF	chr11:47379675-47379750	GM19239	blood:	n/a	n/a
8	CTCF	chr11:47379859-47380023	GM19239	blood:	n/a	n/a
9	FOS	chr11:47381184-47381431	HUVEC	blood vessel:	n/a	n/a
10	GATA2	chr11:47381034-47381345	HUVEC	blood vessel:	n/a	chr11:47381214-47381221 chr11:47381203-47381220 chr11:47381207-47381228 chr11:47381211-47381223
11	HMGN3	chr11:47380336-47380478	K562	blood:	n/a	n/a
12	MAX	chr11:47381155-47381886	NB4	blood:	n/a	n/a
13	MYC	chr11:47378741-47379067	H1-hESC	embryonic stem cell:	n/a	n/a
14	MYC	chr11:47381121-47381753	NB4	blood:	n/a	n/a
15	NFATC1	chr11:47377170-47379243	GM12878	blood:	n/a	n/a
16	NFATC1	chr11:47377156-47379234	GM12878	blood:	n/a	n/a
17	NFATC1	chr11:47379596-47380210	GM12878	blood:	n/a	n/a
18	NFATC1	chr11:47379313-47380198	GM12878	blood:	n/a	n/a
19	NR2C2	chr11:47377334-47379030	Hela-S3	cervix:	n/a	n/a
20	NR2C2	chr11:47379432-47380289	GM12878	blood:	n/a	n/a
21	PBX3	chr11:47377237-47379073	GM12878	blood:	n/a	n/a
22	PBX3	chr11:47379598-47379839	GM12878	blood:	n/a	n/a
23	POLR2A	chr11:47379303-47380376	GM12892	blood:	n/a	n/a
24	POLR2A	chr11:47378277-47379059	GM12878	blood:	n/a	n/a
25	POLR2A	chr11:47377075-47379134	GM12878	blood:	n/a	n/a
26	POLR2A	chr11:47379587-47379998	K562	blood:	n/a	n/a
27	POLR2A	chr11:47381112-47381154	K562	blood:	n/a	n/a
28	POLR2A	chr11:47379369-47380406	GM12878	blood:	n/a	n/a
29	POLR2A	chr11:47377106-47379195	GM12892	blood:	n/a	n/a
30	POLR2A	chr11:47379765-47380172	GM12878	blood:	n/a	n/a
31	POLR2A	chr11:47380762-47380932	K562	blood:	n/a	n/a
32	POLR2A	chr11:47374127-47379189	HL-60	blood:	n/a	n/a
33	POLR2A	chr11:47379329-47382179	HL-60	blood:	n/a	n/a
34	POLR2A	chr11:47377233-47379168	GM12892	blood:	n/a	n/a
35	POLR2A	chr11:47379288-47380403	GM12878	blood:	n/a	n/a
36	POLR2A	chr11:47377122-47379262	GM12892	blood:	n/a	n/a
37	POLR2A	chr11:47379584-47379758	GM12878	blood:	n/a	n/a
38	POLR2A	chr11:47380229-47380230	K562	blood:	n/a	n/a
39	POLR2A	chr11:47379613-47379622	K562	blood:	n/a	n/a
40	POLR2A	chr11:47379389-47380532	K562	blood:	n/a	n/a
41	POLR2A	chr11:47379601-47380023	K562	blood:	n/a	n/a
42	POLR2A	chr11:47377368-47379035	GM12878	blood:	n/a	n/a
43	POLR2A	chr11:47378597-47379126	K562	blood:	n/a	n/a
44	POLR2A	chr11:47378227-47379170	K562	blood:	n/a	n/a
45	POLR2A	chr11:47379367-47380585	GM12878	blood:	n/a	n/a
46	POLR2A	chr11:47379506-47380494	K562	blood:	n/a	n/a
47	POLR2A	chr11:47375214-47379216	HL-60	blood:	n/a	n/a
48	POLR2A	chr11:47378633-47379168	GM12878	blood:	n/a	n/a
49	POLR2A	chr11:47377105-47379138	GM12878	blood:	n/a	n/a
50	POLR2A	chr11:47379632-47380202	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:47380751-47380801	AG09309	skin:	n/a
2	chr11:47380751-47380801	H1-hESC	embryonic stem cell:	embryo
3	chr11:47380751-47380801	ECC-1	luminal epithelium:	n/a
4	chr11:47380751-47380801	ProgFib	skin:	n/a
5	chr11:47380751-47380801	AG09319	gingival:	n/a
6	chr11:47380751-47380801	HRPEpiC	eye:	n/a
7	chr11:47380751-47380801	HCM	heart:	n/a
8	chr11:47380751-47380801	CMK	blood:	n/a
9	chr11:47380751-47380801	HRE	kidney:	n/a
10	chr11:47380751-47380801	NH-A	brain:	n/a
11	chr11:47380751-47380801	BJ	skin:	n/a
12	chr11:47380751-47380801	HUVEC	blood vessel:	n/a
13	chr11:47380751-47380801	SK-N-SH	brain:	n/a
14	chr11:47380751-47380801	HNPCEpiC	eye:	n/a
15	chr11:47380751-47380801	U87	brain:	n/a
16	chr11:47380751-47380801	PANC-1	pancreas:	n/a
17	chr11:47380751-47380801	MCF-7	breast:	n/a
18	chr11:47380751-47380801	GM12891	blood:	n/a
19	chr11:47380751-47380801	NT2-D1	testis:	n/a
20	chr11:47380751-47380801	HCPEpiC	choroid plexus:	n/a
21	chr11:47380751-47380801	RPTEC	kidney:	n/a
22	chr11:47380751-47380801	BE2_C	brain:	n/a
23	chr11:47380751-47380801	SKMC	muscle:	n/a
24	chr11:47380751-47380801	HPAEpiC	pulmonary alveolar:	n/a
25	chr11:47380751-47380801	ovcar-3	ovarian:	n/a
26	chr11:47380751-47380801	GM12892	blood:	n/a
27	chr11:47380751-47380801	HEEpiC	esophagus:	n/a
28	chr11:47380751-47380801	Caco-2	colon:	n/a
29	chr11:47380751-47380801	HCF	heart:	n/a
30	chr11:47380751-47380801	HCT-116	colon:	n/a
31	chr11:47380751-47380801	K562	blood:	n/a
32	chr11:47380751-47380801	AG04450	lung:	fetal
33	chr11:47380751-47380801	T-47D	breast:	n/a
34	chr11:47380751-47380801	Hela-S3	cervix:	n/a
35	chr11:47380751-47380801	IMR90	lung:	fetal
36	chr11:47380751-47380801	HAEpiC	amniotic membrane:	n/a
37	chr11:47380751-47380801	GM12878	blood:	n/a
38	chr11:47380751-47380801	Jurkat	blood:	n/a
39	chr11:47380751-47380801	PFSK-1	brain:	n/a
40	chr11:47380751-47380801	HL-60	blood:	n/a
41	chr11:47380751-47380801	AG04449	skin:	fetal
42	chr11:47380751-47380801	SAEC	small airway:	n/a
43	chr11:47380751-47380801	PrEC	prostate:	n/a
44	chr11:47380751-47380801	NHBE	bronchial:	n/a
45	chr11:47380751-47380801	Hepatocyte	liver:	n/a
46	chr11:47380751-47380801	HRCEpiC	kidney:	n/a
47	chr11:47380751-47380801	SK-N-MC	brain:	n/a
48	chr11:47380751-47380801	AG10803	skin:	n/a
49	chr11:47380751-47380801	HIPEpiC	eye:	n/a
50	chr11:47380751-47380801	A549	lung:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:47195702..47198669-chr11:47379540..47381275,2	K562	blood:
2	chr11:47378071..47380550-chr11:47420446..47422509,2	MCF-7	breast:
3	chr11:47369216..47372065-chr11:47378496..47380430,2	K562	blood:
4	chr11:47372212..47375004-chr11:47380040..47382047,2	MCF-7	breast:
5	chr11:47380057..47381801-chr11:47388110..47390294,2	K562	blood:
6	chr11:47362680..47364496-chr11:47377424..47380369,2	K562	blood:
7	chr11:47376723..47380459-chr11:47382736..47386696,5	K562	blood:
8	chr11:47376739..47379188-chr11:47381497..47383536,3	MCF-7	breast:
9	chr11:47379032..47381068-chr11:47385092..47386815,2	MCF-7	breast:
10	chr11:47380338..47382124-chr11:47391375..47394972,3	K562	blood:
11	chr11:47381478..47383023-chr11:47384952..47387041,2	K562	blood:
12	chr11:47269295..47270881-chr11:47376927..47379206,2	MCF-7	breast:
13	chr11:47376739..47379188-chr11:47381497..47383536,3	MCF-7	breast:
14	chr11:47284615..47286154-chr11:47378309..47380151,2	MCF-7	breast:
15	chr11:47377126..47379230-chr11:47428179..47431168,2	MCF-7	breast:
16	chr11:47290509..47292951-chr11:47377343..47380007,3	MCF-7	breast:

No data

Variant related genes	Relation type
MYBPC3	TF binding region
MYBPC3	CpG island
ENSG00000134575	chromatin interactions
ENSG00000255197	chromatin interactions
ENSG00000165915	chromatin interactions
ENSG00000149182	chromatin interactions
ENSG00000025434	chromatin interactions
ENSG00000110514	chromatin interactions
ENSG00000134571	chromatin interactions

Extended variants
information (count: 154 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:154 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545261246	chr11:47379026-47379027	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs538279687	chr11:47379033-47379034	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs538953023	chr11:47379055-47379056	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs5791758	chr11:47379060-47379061	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs558941470	chr11:47379102-47379103	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs575525505	chr11:47379103-47379104	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs538360525	chr11:47379125-47379126	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs35600396	chr11:47379128-47379129	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs375828460	chr11:47379129-47379130	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs568835274	chr11:47379150-47379151	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs573511349	chr11:47379152-47379153	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs147807448	chr11:47379170-47379171	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs559119397	chr11:47379210-47379211	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs11039199	chr11:47379212-47379213	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs146949395	chr11:47379246-47379247	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs564923448	chr11:47379273-47379274	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs534615776	chr11:47379276-47379277	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs530390851	chr11:47379285-47379286	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs550660139	chr11:47379289-47379290	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs560917896	chr11:47379303-47379304	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs148351292	chr11:47379313-47379314	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs547254683	chr11:47379314-47379315	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs567052433	chr11:47379336-47379337	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs539344972	chr11:47379353-47379354	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs34206625	chr11:47379383-47379384	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs552568522	chr11:47379396-47379397	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs2084946	chr11:47379407-47379408	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs113123267	chr11:47379410-47379411	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs554648209	chr11:47379411-47379412	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs534119431	chr11:47379412-47379413	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs554075534	chr11:47379416-47379417	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs534021311	chr11:47379418-47379419	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs552783406	chr11:47379436-47379437	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs200490073	chr11:47379443-47379444	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs370728046	chr11:47379454-47379455	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs572681011	chr11:47379455-47379456	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs141498481	chr11:47379456-47379457	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs546055676	chr11:47379497-47379498	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs574699834	chr11:47379502-47379503	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs558531149	chr11:47379520-47379521	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs556150222	chr11:47379525-47379526	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs189171582	chr11:47379536-47379537	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs377658810	chr11:47379538-47379539	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs371132835	chr11:47379570-47379571	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs576312136	chr11:47379609-47379610	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs1542321	chr11:47379615-47379616	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs11039200	chr11:47379646-47379647	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs560686734	chr11:47379737-47379738	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs370494195	chr11:47379749-47379750	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs367679981	chr11:47379762-47379763	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Medulloblastoma	16783165	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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:132 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:47371000-47379800	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr11:47374800-47380400	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr11:47375400-47379600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
4	chr11:47375400-47381000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr11:47375600-47379600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr11:47375600-47380400	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr11:47375600-47380600	Strong transcription	Primary B cells from cord blood	blood
8	chr11:47375600-47381000	Strong transcription	Primary B cells from peripheral blood	blood
9	chr11:47376200-47380200	Strong transcription	Primary hematopoietic stem cells	blood
10	chr11:47376800-47381400	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr11:47377200-47386600	Weak transcription	Right Atrium	heart
12	chr11:47377200-47391400	Weak transcription	Psoas Muscle	Psoas
13	chr11:47377200-47397800	Weak transcription	Fetal Muscle Leg	muscle
14	chr11:47377400-47380400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
15	chr11:47377600-47380200	Strong transcription	Rectal Mucosa Donor 29	rectum
16	chr11:47377600-47380800	Weak transcription	Brain Hippocampus Middle	brain
17	chr11:47377600-47381000	Weak transcription	Duodenum Mucosa	Duodenum
18	chr11:47377600-47381000	Weak transcription	Placenta	Placenta
19	chr11:47377600-47396800	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr11:47377600-47397600	Weak transcription	Brain Cingulate Gyrus	brain
21	chr11:47377600-47397800	Weak transcription	Brain Substantia Nigra	brain
22	chr11:47377800-47379400	Weak transcription	Rectal Smooth Muscle	rectum
23	chr11:47377800-47379400	Weak transcription	Right Ventricle	heart
24	chr11:47377800-47379800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr11:47377800-47379800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr11:47377800-47380200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr11:47377800-47380800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
28	chr11:47377800-47382200	Weak transcription	Colon Smooth Muscle	Colon
29	chr11:47377800-47382600	Weak transcription	Fetal Heart	heart
30	chr11:47377800-47382800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr11:47378000-47380000	Strong transcription	Skeletal Muscle Male	skeletal muscle
32	chr11:47378000-47380200	Strong transcription	Skeletal Muscle Female	skeletal muscle
33	chr11:47378000-47381400	Weak transcription	Colonic Mucosa	Colon
34	chr11:47378200-47379800	Strong transcription	Brain Anterior Caudate	brain
35	chr11:47378200-47380200	Strong transcription	Stomach Smooth Muscle	stomach
36	chr11:47378400-47379800	Strong transcription	Spleen	Spleen
37	chr11:47378400-47380200	Strong transcription	Brain Inferior Temporal Lobe	brain
38	chr11:47378400-47381400	Weak transcription	Fetal Intestine Small	intestine
39	chr11:47378600-47381400	Weak transcription	Pancreas	Pancrea
40	chr11:47378600-47382000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr11:47378800-47379200	Genic enhancers	Gastric	stomach
42	chr11:47378800-47381600	Weak transcription	Fetal Lung	lung
43	chr11:47378800-47381800	Weak transcription	Adipose Nuclei	Adipose
44	chr11:47378800-47393400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr11:47379000-47379400	Weak transcription	Fetal Kidney	kidney
46	chr11:47379000-47379600	Weak transcription	GM12878-XiMat	blood
47	chr11:47379000-47379800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr11:47379200-47379800	Strong transcription	Gastric	stomach
49	chr11:47379400-47380000	Active TSS	Fetal Kidney	kidney
50	chr11:47379400-47380000	Genic enhancers	Right Ventricle	heart

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