Variant report

Variant	esv3320420
Chromosome Location	chr1:92230064-92235262
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	chr1:92235102-92235184	K562	blood:	n/a	n/a
2	ATF1	chr1:92231509-92231735	K562	blood:	n/a	n/a
3	BHLHE40	chr1:92234966-92235192	K562	blood:	n/a	n/a
4	CBX3	chr1:92234830-92235214	K562	blood:	n/a	n/a
5	CEBPB	chr1:92231492-92231777	K562	blood:	n/a	chr1:92231639-92231650
6	CEBPB	chr1:92231495-92231736	HepG2	liver:	n/a	chr1:92231639-92231650
7	CEBPB	chr1:92231531-92231745	IMR90	lung:	n/a	chr1:92231639-92231650
8	CEBPB	chr1:92231054-92232006	K562	blood:	n/a	chr1:92231639-92231650
9	CEBPB	chr1:92231440-92231861	K562	blood:	n/a	chr1:92231639-92231650
10	CEBPB	chr1:92230892-92231782	Hela-S3	cervix:	n/a	chr1:92231639-92231650
11	CEBPD	chr1:92231416-92231886	K562	blood:	n/a	n/a
12	CEBPD	chr1:92231510-92231917	K562	blood:	n/a	n/a
13	CHD2	chr1:92230934-92231199	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr1:92235180-92235353	K562	blood:	n/a	n/a
15	CTCF	chr1:92230120-92230270	HMF	breast:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
16	CTCF	chr1:92230060-92230210	K562	blood:	n/a	n/a
17	CTCF	chr1:92229984-92230364	H1-hESC	embryonic stem cell:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
18	CTCF	chr1:92230153-92230246	GM12891	blood:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
19	CTCF	chr1:92229983-92230292	H1-hESC	embryonic stem cell:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
20	CTCF	chr1:92230053-92230283	H1-hESC	embryonic stem cell:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
21	CTCF	chr1:92230140-92230290	BE2_C	brain:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
22	CTCF	chr1:92230172-92230282	Hela-S3	cervix:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
23	CTCF	chr1:92229990-92230332	K562	blood:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
24	CTCF	chr1:92230180-92230228	Fibrobl	skin:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
25	CTCF	chr1:92230260-92230410	A549	lung:	n/a	n/a
26	CTCF	chr1:92230140-92230290	HepG2	liver:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
27	CTCF	chr1:92230100-92230250	HBMEC	blood vessel:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
28	CTCF	chr1:92230114-92230301	ProgFib	skin:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
29	CTCF	chr1:92229989-92230373	K562	blood:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
30	CTCF	chr1:92230100-92230250	WERI-Rb-1	eye:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
31	CTCF	chr1:92230140-92230290	HCPEpiC	choroid plexus:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
32	CTCF	chr1:92230180-92230330	BE2_C	brain:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
33	CTCF	chr1:92230120-92230270	HCPEpiC	choroid plexus:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
34	CTCF	chr1:92230111-92230324	K562	blood:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
35	CTCF	chr1:92230050-92230301	K562	blood:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
36	CTCF	chr1:92229987-92230389	K562	blood:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
37	CTCF	chr1:92230100-92230250	Caco-2	colon:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
38	CTCF	chr1:92230198-92230239	GM19239	blood:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
39	CTCF	chr1:92230150-92230151	GM12891	blood:	n/a	n/a
40	CTCF	chr1:92230188-92230196	GM19239	blood:	n/a	n/a
41	CTCF	chr1:92230180-92230330	Hela-S3	cervix:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
42	CTCF	chr1:92230203-92230226	A549	lung:	n/a	chr1:92230204-92230217
43	CTCF	chr1:92230120-92230270	SK-N-SH_RA	brain:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
44	CTCF	chr1:92230140-92230290	HBMEC	blood vessel:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
45	CTCF	chr1:92230120-92230270	WERI-Rb-1	eye:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
46	EGR1	chr1:92229998-92230318	K562	blood:	n/a	chr1:92230170-92230181
47	EGR1	chr1:92229950-92230361	H1-hESC	embryonic stem cell:	n/a	chr1:92230170-92230181
48	EGR1	chr1:92230002-92230317	K562	blood:	n/a	chr1:92230170-92230181
49	ELF1	chr1:92234832-92235147	K562	blood:	n/a	n/a
50	EP300	chr1:92234998-92235229	K562	blood:	n/a	chr1:92235197-92235211

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:92234946-92234996	BE2_C	brain:	n/a
2	chr1:92234946-92234996	GM19239	blood:	n/a
3	chr1:92234946-92234996	NT2-D1	testis:	n/a
4	chr1:92234946-92234996	H1-hESC	embryonic stem cell:	embryo
5	chr1:92234946-92234996	Hela-S3	cervix:	n/a
6	chr1:92234946-92234996	HRPEpiC	eye:	n/a
7	chr1:92234946-92234996	CMK	blood:	n/a
8	chr1:92234946-92234996	SK-N-SH_RA	brain:	n/a
9	chr1:92234946-92234996	A549	lung:	n/a
10	chr1:92234946-92234996	HCT-116	colon:	n/a
11	chr1:92234946-92234996	LNCaP	prostate:	n/a
12	chr1:92234946-92234996	AG09309	skin:	n/a
13	chr1:92234946-92234996	PrEC	prostate:	n/a
14	chr1:92234946-92234996	IMR90	lung:	fetal
15	chr1:92234946-92234996	SK-N-MC	brain:	n/a
16	chr1:92234946-92234996	HCM	heart:	n/a
17	chr1:92234946-92234996	K562	blood:	n/a
18	chr1:92234946-92234996	RPTEC	kidney:	n/a
19	chr1:92234946-92234996	HMEC	breast:	n/a
20	chr1:92234946-92234996	ECC-1	luminal epithelium:	n/a
21	chr1:92234946-92234996	SAEC	small airway:	n/a
22	chr1:92234946-92234996	ProgFib	skin:	n/a
23	chr1:92234946-92234996	HAEpiC	amniotic membrane:	n/a
24	chr1:92234946-92234996	MCF10A-Er-Src	breast:	n/a
25	chr1:92234946-92234996	GM12892	blood:	n/a
26	chr1:92234946-92234996	AG09319	gingival:	n/a
27	chr1:92234946-92234996	Jurkat	blood:	n/a
28	chr1:92234946-92234996	ovcar-3	ovarian:	n/a
29	chr1:92234946-92234996	HRE	kidney:	n/a
30	chr1:92234946-92234996	HCF	heart:	n/a
31	chr1:92234946-92234996	AG04449	skin:	fetal
32	chr1:92234946-92234996	AoSMC	blood vessel:	n/a
33	chr1:92234946-92234996	NB4	blood:	n/a
34	chr1:92234946-92234996	HUVEC	blood vessel:	n/a
35	chr1:92234946-92234996	HRCEpiC	kidney:	n/a
36	chr1:92234946-92234996	HepG2	liver:	n/a
37	chr1:92234946-92234996	HEK293	kidney:	embryo
38	chr1:92234946-92234996	BJ	skin:	n/a
39	chr1:92234946-92234996	NHDF-neo	bronchial:	n/a
40	chr1:92234946-92234996	AG04450	lung:	fetal
41	chr1:92234946-92234996	MCF-7	breast:	n/a
42	chr1:92234946-92234996	HPAEpiC	pulmonary alveolar:	n/a
43	chr1:92234946-92234996	AG10803	skin:	n/a
44	chr1:92234946-92234996	Caco-2	colon:	n/a
45	chr1:92234946-92234996	Hepatocyte	liver:	n/a
46	chr1:92234946-92234996	SK-N-SH	brain:	n/a
47	chr1:92234946-92234996	SKMC	muscle:	n/a
48	chr1:92234946-92234996	GM06990	blood:	n/a
49	chr1:92234946-92234996	HNPCEpiC	eye:	n/a
50	chr1:92234946-92234996	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:92232541..92234077-chr1:92245076..92247021,2	K562	blood:
2	chr1:92231081..92233303-chr1:92233328..92236066,2	K562	blood:
3	chr1:92217896..92221069-chr1:92227993..92231134,3	K562	blood:
4	chr1:92226383..92229371-chr1:92235062..92236732,2	K562	blood:
5	chr1:92196718..92198594-chr1:92235219..92237131,2	K562	blood:

Variant related genes	Relation type
TGFBR3	TF binding region
TGFBR3	CpG island
ENSG00000069702	chromatin interactions

Extended variants
information (count: 187 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:187 , 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	rs537622927	chr1:92230071-92230072	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs114999027	chr1:92230074-92230075	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529672551	chr1:92230100-92230101	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564886971	chr1:92230116-92230117	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570550639	chr1:92230131-92230132	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188811217	chr1:92230147-92230148	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs114313116	chr1:92230159-92230160	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs193206625	chr1:92230160-92230161	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183955946	chr1:92230184-92230185	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570601961	chr1:92230206-92230207	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530565616	chr1:92230207-92230208	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs188238283	chr1:92230290-92230291	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs6670338	chr1:92230305-92230306	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs572708466	chr1:92230352-92230353	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs78740513	chr1:92230365-92230366	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs181380014	chr1:92230366-92230367	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs140966270	chr1:92230368-92230369	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576364159	chr1:92230369-92230370	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs376056513	chr1:92230412-92230413	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544074214	chr1:92230449-92230450	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs371609948	chr1:92230472-92230473	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs11807110	chr1:92230498-92230499	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs150248773	chr1:92230531-92230532	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540778546	chr1:92230541-92230542	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559444175	chr1:92230607-92230608	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs72716409	chr1:92230626-92230627	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs184076430	chr1:92230669-92230670	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs550681252	chr1:92230694-92230695	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs116755186	chr1:92230711-92230712	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs375630742	chr1:92230714-92230715	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs79325665	chr1:92230770-92230771	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530740797	chr1:92230883-92230884	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs189740272	chr1:92230908-92230909	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570566742	chr1:92230964-92230965	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs528246666	chr1:92231007-92231008	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546388391	chr1:92231052-92231053	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565878888	chr1:92231084-92231085	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs575187788	chr1:92231112-92231113	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs572112677	chr1:92231130-92231131	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs554574249	chr1:92231141-92231142	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs75475379	chr1:92231162-92231163	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs537361739	chr1:92231173-92231174	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs59197518	chr1:92231239-92231240	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs577369063	chr1:92231247-92231248	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs186824372	chr1:92231264-92231265	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs114066736	chr1:92231265-92231266	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs114422669	chr1:92231307-92231308	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs12044500	chr1:92231325-92231326	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs563292730	chr1:92231338-92231339	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs191983065	chr1:92231350-92231351	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	16397240	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:213 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92204800-92247000	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr1:92208400-92235800	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr1:92211800-92235600	Weak transcription	Fetal Kidney	kidney
4	chr1:92213800-92235000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr1:92215200-92232400	Weak transcription	A549	lung
6	chr1:92216800-92241800	Weak transcription	Aorta	Aorta
7	chr1:92217200-92230200	Weak transcription	Pancreas	Pancrea
8	chr1:92217400-92232400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr1:92217600-92230200	Weak transcription	Hela-S3	cervix
10	chr1:92217800-92247800	Weak transcription	Small Intestine	intestine
11	chr1:92219400-92238200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr1:92220400-92234000	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr1:92220600-92255800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr1:92221000-92248000	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr1:92222200-92231000	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr1:92223800-92232000	Enhancers	K562	blood
17	chr1:92224400-92242800	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr1:92224800-92234400	Weak transcription	Right Ventricle	heart
19	chr1:92225200-92232000	Weak transcription	Brain Cingulate Gyrus	brain
20	chr1:92225200-92235000	Weak transcription	Brain Hippocampus Middle	brain
21	chr1:92225400-92234400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr1:92225400-92241600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr1:92226000-92230600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr1:92226400-92231200	Enhancers	Fetal Heart	heart
25	chr1:92226600-92236400	Weak transcription	Brain Substantia Nigra	brain
26	chr1:92226800-92232000	Enhancers	Placenta	Placenta
27	chr1:92227000-92257200	Weak transcription	Fetal Intestine Small	intestine
28	chr1:92227200-92230800	Weak transcription	Liver	Liver
29	chr1:92227200-92234600	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr1:92227200-92234800	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr1:92227400-92230200	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr1:92227400-92230600	Genic enhancers	NHDF-Ad	bronchial
33	chr1:92227800-92235400	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr1:92228400-92231200	Enhancers	Fetal Lung	lung
35	chr1:92228600-92230200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr1:92228600-92230200	Enhancers	Fetal Muscle Leg	muscle
37	chr1:92228600-92230200	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr1:92228600-92235200	Weak transcription	Colon Smooth Muscle	Colon
39	chr1:92228800-92230200	Enhancers	Right Atrium	heart
40	chr1:92229200-92231200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr1:92229200-92232400	Genic enhancers	HepG2	liver
42	chr1:92229200-92241600	Weak transcription	Esophagus	oesophagus
43	chr1:92229400-92230200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr1:92229400-92230400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr1:92229400-92230400	Weak transcription	Psoas Muscle	Psoas
46	chr1:92229400-92230600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr1:92229400-92230800	Weak transcription	Adipose Nuclei	Adipose
48	chr1:92229400-92235200	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr1:92229800-92230400	Enhancers	Osteobl	bone
50	chr1:92229800-92230600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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