Variant report

Variant	nsv467743
Chromosome Location	chr11:23783338-23841175
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	chr11:23808741-23808892	HepG2	liver:	n/a	n/a
2	BRCA1	chr11:23791141-23791164	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr11:23829111-23829319	K562	blood:	n/a	chr11:23829233-23829244
4	CEBPB	chr11:23820766-23821130	IMR90	lung:	n/a	chr11:23821104-23821117
5	CEBPB	chr11:23820772-23821109	A549	lung:	n/a	n/a
6	CEBPB	chr11:23829064-23829390	IMR90	lung:	n/a	chr11:23829233-23829244
7	CEBPB	chr11:23808790-23808947	HepG2	liver:	n/a	chr11:23808906-23808917
8	CEBPB	chr11:23829075-23829384	HepG2	liver:	n/a	chr11:23829233-23829244
9	CEBPB	chr11:23794359-23794613	HepG2	liver:	n/a	chr11:23794482-23794495 chr11:23794482-23794493
10	CEBPB	chr11:23820809-23821124	HepG2	liver:	n/a	chr11:23821104-23821117
11	CEBPB	chr11:23829094-23829349	A549	lung:	n/a	chr11:23829233-23829244
12	CHD1	chr11:23789645-23789701	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr11:23827236-23827314	ProgFib	skin:	n/a	n/a
14	CUX1	chr11:23796276-23796354	GM12878	blood:	n/a	n/a
15	E2F4	chr11:23817236-23817375	MCF10A-Er-Src	breast:	n/a	n/a
16	E2F4	chr11:23825851-23826211	MCF10A-Er-Src	breast:	n/a	n/a
17	EP300	chr11:23799370-23800076	SK-N-SH	brain:	n/a	chr11:23799711-23799719 chr11:23799808-23799822 chr11:23799387-23799401
18	EP300	chr11:23799526-23799734	SK-N-SH_RA	brain:	n/a	chr11:23799711-23799719
19	EP300	chr11:23831012-23831466	SK-N-SH_RA	brain:	n/a	n/a
20	EP300	chr11:23831030-23831481	SK-N-SH_RA	brain:	n/a	n/a
21	EP300	chr11:23811357-23811712	SK-N-SH_RA	brain:	n/a	chr11:23811539-23811548
22	EP300	chr11:23811383-23811725	SK-N-SH_RA	brain:	n/a	chr11:23811539-23811548
23	EP300	chr11:23800514-23801018	ECC-1	luminal epithelium:	n/a	n/a
24	ESR1	chr11:23805948-23806264	ECC-1	luminal epithelium:	n/a	n/a
25	ESR1	chr11:23805965-23806220	ECC-1	luminal epithelium:	n/a	n/a
26	FOS	chr11:23811393-23811656	MCF10A-Er-Src	breast:	n/a	chr11:23811538-23811548 chr11:23811538-23811547 chr11:23811539-23811548 chr11:23811539-23811546 chr11:23811537-23811548 chr11:23811537-23811549 chr11:23811538-23811548
27	FOS	chr11:23811386-23811705	MCF10A-Er-Src	breast:	n/a	chr11:23811538-23811548 chr11:23811538-23811547 chr11:23811539-23811548 chr11:23811539-23811546 chr11:23811537-23811548 chr11:23811537-23811549 chr11:23811538-23811548
28	FOS	chr11:23811420-23811620	MCF10A-Er-Src	breast:	n/a	chr11:23811538-23811548 chr11:23811538-23811547 chr11:23811539-23811548 chr11:23811539-23811546 chr11:23811537-23811548 chr11:23811537-23811549 chr11:23811538-23811548
29	FOS	chr11:23811390-23811563	MCF10A-Er-Src	breast:	n/a	chr11:23811538-23811548 chr11:23811538-23811547 chr11:23811539-23811548 chr11:23811539-23811546 chr11:23811537-23811548 chr11:23811537-23811549 chr11:23811538-23811548
30	FOS	chr11:23811368-23811731	HUVEC	blood vessel:	n/a	chr11:23811538-23811548 chr11:23811538-23811547 chr11:23811539-23811548 chr11:23811539-23811546 chr11:23811537-23811548 chr11:23811537-23811549 chr11:23811538-23811548
31	FOSL2	chr11:23811335-23811663	HepG2	liver:	n/a	chr11:23811538-23811548 chr11:23811538-23811547 chr11:23811539-23811548 chr11:23811539-23811546 chr11:23811537-23811549 chr11:23811538-23811548
32	FOSL2	chr11:23811325-23811829	SK-N-SH	brain:	n/a	chr11:23811538-23811548 chr11:23811538-23811547 chr11:23811539-23811548 chr11:23811539-23811546 chr11:23811537-23811549 chr11:23811538-23811548
33	FOSL2	chr11:23811291-23811706	A549	lung:	n/a	chr11:23811538-23811548 chr11:23811538-23811547 chr11:23811539-23811548 chr11:23811539-23811546 chr11:23811537-23811549 chr11:23811538-23811548
34	FOXA1	chr11:23808573-23808937	HepG2	liver:	n/a	n/a
35	FOXA1	chr11:23808616-23808873	HepG2	liver:	n/a	n/a
36	FOXA1	chr11:23808562-23808968	HepG2	liver:	n/a	n/a
37	FOXA1	chr11:23808603-23808878	HepG2	liver:	n/a	n/a
38	FOXA2	chr11:23808652-23808868	HepG2	liver:	n/a	n/a
39	FOXM1	chr11:23800440-23801058	ECC-1	luminal epithelium:	n/a	n/a
40	GATA3	chr11:23811222-23811921	SK-N-SH	brain:	n/a	chr11:23811644-23811653 chr11:23811540-23811549 chr11:23811313-23811323
41	GATA3	chr11:23823719-23823970	SH-SY5Y	brain:	n/a	n/a
42	GATA3	chr11:23831175-23831759	SH-SY5Y	brain:	n/a	n/a
43	GATA3	chr11:23799378-23799847	SK-N-SH	brain:	n/a	n/a
44	GATA3	chr11:23799575-23799772	SH-SY5Y	brain:	n/a	n/a
45	GATA3	chr11:23811376-23811931	SK-N-SH	brain:	n/a	chr11:23811644-23811653 chr11:23811540-23811549
46	GATA3	chr11:23807067-23807774	MCF-7	breast:	n/a	chr11:23807303-23807312
47	GATA3	chr11:23784997-23785125	SH-SY5Y	brain:	n/a	n/a
48	GATA3	chr11:23816729-23816906	SH-SY5Y	brain:	n/a	n/a
49	HDAC2	chr11:23807303-23807522	MCF-7	breast:	n/a	n/a
50	HNF4A	chr11:23808520-23808830	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:23811425-23811475	MCF10A-Er-Src	breast:	n/a
2	chr11:23811425-23811475	AoSMC	blood vessel:	n/a
3	chr11:23811425-23811475	HEK293	kidney:	embryo
4	chr11:23811425-23811475	NT2-D1	testis:	n/a
5	chr11:23811425-23811475	HRE	kidney:	n/a
6	chr11:23811425-23811475	HCM	heart:	n/a
7	chr11:23811425-23811475	SK-N-SH_RA	brain:	n/a
8	chr11:23811425-23811475	HCF	heart:	n/a
9	chr11:23811425-23811475	GM19239	blood:	n/a
10	chr11:23811425-23811475	NB4	blood:	n/a
11	chr11:23811425-23811475	AG04450	lung:	fetal
12	chr11:23811425-23811475	IMR90	lung:	fetal
13	chr11:23811425-23811475	SAEC	small airway:	n/a
14	chr11:23811425-23811475	HRPEpiC	eye:	n/a
15	chr11:23811425-23811475	Hepatocyte	liver:	n/a
16	chr11:23811425-23811475	HPAEpiC	pulmonary alveolar:	n/a
17	chr11:23811425-23811475	T-47D	breast:	n/a
18	chr11:23811425-23811475	HEEpiC	esophagus:	n/a
19	chr11:23811425-23811475	MCF-7	breast:	n/a
20	chr11:23811425-23811475	GM12891	blood:	n/a
21	chr11:23811425-23811475	Hela-S3	cervix:	n/a
22	chr11:23811425-23811475	CMK	blood:	n/a
23	chr11:23811425-23811475	GM12878	blood:	n/a
24	chr11:23811425-23811475	GM12892	blood:	n/a
25	chr11:23811425-23811475	ECC-1	luminal epithelium:	n/a
26	chr11:23811425-23811475	NHDF-neo	bronchial:	n/a
27	chr11:23811425-23811475	SKMC	muscle:	n/a
28	chr11:23811425-23811475	AG10803	skin:	n/a
29	chr11:23811425-23811475	NHBE	bronchial:	n/a
30	chr11:23811425-23811475	HMEC	breast:	n/a
31	chr11:23811425-23811475	HAEpiC	amniotic membrane:	n/a
32	chr11:23811425-23811475	ovcar-3	ovarian:	n/a
33	chr11:23811425-23811475	SK-N-MC	brain:	n/a
34	chr11:23811425-23811475	PANC-1	pancreas:	n/a
35	chr11:23811425-23811475	HCT-116	colon:	n/a
36	chr11:23811425-23811475	A549	lung:	n/a
37	chr11:23811425-23811475	AG09319	gingival:	n/a
38	chr11:23811425-23811475	PFSK-1	brain:	n/a
39	chr11:23811425-23811475	LNCaP	prostate:	n/a
40	chr11:23811425-23811475	SK-N-SH	brain:	n/a
41	chr11:23811425-23811475	HUVEC	blood vessel:	n/a
42	chr11:23811425-23811475	NH-A	brain:	n/a
43	chr11:23811425-23811475	HCPEpiC	choroid plexus:	n/a
44	chr11:23811425-23811475	U87	brain:	n/a
45	chr11:23811425-23811475	ProgFib	skin:	n/a
46	chr11:23811425-23811475	HepG2	liver:	n/a
47	chr11:23811425-23811475	K562	blood:	n/a
48	chr11:23811425-23811475	Caco-2	colon:	n/a
49	chr11:23811425-23811475	Jurkat	blood:	n/a
50	chr11:23811425-23811475	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:23822728..23824994-chr11:23830826..23833587,2	K562	blood:
2	chr11:23822728..23824994-chr11:23830826..23833587,2	K562	blood:
3	chr11:23798376..23799116-chr5:32449587..32450235,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-17A1.2.1-2	chr11:23829736-23829778	XLOC_009395
2	lnc-LUZP2-1	chr11:23816369-23816430	ENSG00000255193
3	lnc-LUZP2-1	chr11:23818254-23818516	ENSG00000255193
4	lnc-RP11-17A1.2.1-2	chr11:23789323-23789362	XLOC_009394
5	lnc-RP11-17A1.2.1-2	chr11:23826025-23826144	ENSG00000254861
6	lnc-RP11-17A1.2.1-2	chr11:23802334-23802418	ENSG00000254861
7	lnc-RP11-17A1.2.1-5	chr11:23818256-23819005	NONHSAT018430
8	lnc-RP11-17A1.2.1-5	chr11:23817463-23817487	NONHSAT018430
9	lnc-RP11-17A1.2.1-2	chr11:23826000-23826222	XLOC_009395

Variant related genes	Relation type
ENSG00000254861	TF binding region
ENSG00000254861	CpG island

Extended variants
information (count: 1855 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1855 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4923127	chr11:23783338-23783339	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574384175	chr11:23783385-23783386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs549697791	chr11:23783436-23783437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147723561	chr11:23783439-23783440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529121028	chr11:23783465-23783466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553832267	chr11:23783469-23783470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs186320105	chr11:23783474-23783475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541646651	chr11:23783499-23783500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568473734	chr11:23783558-23783559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534240637	chr11:23783587-23783588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547834613	chr11:23783597-23783598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73439901	chr11:23783608-23783609	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs539828294	chr11:23783619-23783620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572426174	chr11:23783655-23783656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556606919	chr11:23783665-23783666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs142498691	chr11:23783726-23783727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191230451	chr11:23783729-23783730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs61876078	chr11:23783736-23783737	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs571829298	chr11:23783743-23783744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540688560	chr11:23783772-23783773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs56797973	chr11:23783788-23783789	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs564184733	chr11:23783795-23783796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540122643	chr11:23783835-23783836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140521785	chr11:23783875-23783876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs57577755	chr11:23783881-23783882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577243900	chr11:23783886-23783887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs77995638	chr11:23783887-23783888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs60922886	chr11:23783929-23783930	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs181572221	chr11:23783932-23783933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548910416	chr11:23783968-23783969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs146905892	chr11:23783978-23783979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534914336	chr11:23783987-23783988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs565170451	chr11:23784020-23784021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185305312	chr11:23784038-23784039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189960970	chr11:23784057-23784058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539889342	chr11:23784058-23784059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549086245	chr11:23784062-23784063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs60859127	chr11:23784063-23784064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550107411	chr11:23784071-23784072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs570256851	chr11:23784074-23784075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs59956121	chr11:23784079-23784080	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs555696782	chr11:23784118-23784119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs61876079	chr11:23784132-23784133	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs114781719	chr11:23784167-23784168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557474038	chr11:23784184-23784185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577307650	chr11:23784266-23784267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs113858815	chr11:23784378-23784379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs61499360	chr11:23784389-23784390	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs573876483	chr11:23784391-23784392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs542875211	chr11:23784419-23784420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
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
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Renal cell carcinoma	18194544	CNVD
Myelofibrosis	22110671	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Autism	22102821	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:23781400-23785400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr11:23781400-23787200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr11:23785400-23789000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr11:23786200-23786400	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr11:23787000-23788200	Enhancers	Placenta Amnion	Placenta Amnion
6	chr11:23787200-23788000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr11:23787200-23788000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr11:23787200-23788200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr11:23789200-23792000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr11:23790200-23791200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
11	chr11:23790400-23791800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
12	chr11:23792600-23794200	Enhancers	Fetal Stomach	stomach
13	chr11:23792800-23794200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr11:23794200-23795200	Weak transcription	Fetal Stomach	stomach
15	chr11:23795200-23795400	Enhancers	Fetal Stomach	stomach
16	chr11:23798600-23799200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr11:23799200-23803200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr11:23799600-23802400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr11:23800400-23802000	Enhancers	NH-A	brain
20	chr11:23800600-23802600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr11:23800800-23801200	Enhancers	HSMM	muscle
22	chr11:23801200-23811000	Weak transcription	HSMM	muscle
23	chr11:23803200-23803600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr11:23803600-23804600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr11:23804600-23806800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr11:23805200-23806400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr11:23805800-23806200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr11:23806200-23811200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:23806400-23806600	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr11:23806400-23807000	Enhancers	HepG2	liver
31	chr11:23806600-23806800	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr11:23806800-23808200	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr11:23806800-23808200	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr11:23807000-23808000	Weak transcription	HepG2	liver
35	chr11:23807000-23809000	Enhancers	Fetal Intestine Small	intestine
36	chr11:23807400-23808600	Enhancers	Fetal Lung	lung
37	chr11:23807800-23809400	Enhancers	Stomach Mucosa	stomach
38	chr11:23808000-23809400	Enhancers	Fetal Intestine Large	intestine
39	chr11:23808000-23809600	Enhancers	HepG2	liver
40	chr11:23808200-23809000	Enhancers	Gastric	stomach
41	chr11:23808200-23809000	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr11:23808200-23809600	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr11:23808800-23809000	Enhancers	Pancreas	Pancrea
44	chr11:23809000-23810600	Weak transcription	Fetal Intestine Small	intestine
45	chr11:23809000-23810600	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr11:23809400-23810600	Weak transcription	Fetal Intestine Large	intestine
47	chr11:23809400-23810600	Weak transcription	Pancreas	Pancrea
48	chr11:23809400-23810600	Weak transcription	Stomach Mucosa	stomach
49	chr11:23809600-23810400	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr11:23809600-23810600	Weak transcription	HepG2	liver

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