Variant report

Variant	esv988308
Chromosome Location	chr1:92227910-92236935
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	chr1:92228764-92229274	K562	blood:	n/a	n/a
2	ARID3A	chr1:92235102-92235184	K562	blood:	n/a	n/a
3	ATF1	chr1:92228791-92229259	K562	blood:	n/a	n/a
4	ATF1	chr1:92231509-92231735	K562	blood:	n/a	n/a
5	BACH1	chr1:92228760-92228893	K562	blood:	n/a	n/a
6	BHLHE40	chr1:92234966-92235192	K562	blood:	n/a	n/a
7	BHLHE40	chr1:92228990-92229283	K562	blood:	n/a	n/a
8	CBX3	chr1:92234830-92235214	K562	blood:	n/a	n/a
9	CCNT2	chr1:92228802-92229416	K562	blood:	n/a	n/a
10	CEBPB	chr1:92231531-92231745	IMR90	lung:	n/a	chr1:92231639-92231650
11	CEBPB	chr1:92228782-92229174	IMR90	lung:	n/a	chr1:92228905-92228918
12	CEBPB	chr1:92231054-92232006	K562	blood:	n/a	chr1:92231639-92231650
13	CEBPB	chr1:92228774-92229149	K562	blood:	n/a	chr1:92228905-92228918
14	CEBPB	chr1:92230892-92231782	Hela-S3	cervix:	n/a	chr1:92231639-92231650
15	CEBPB	chr1:92231440-92231861	K562	blood:	n/a	chr1:92231639-92231650
16	CEBPB	chr1:92231492-92231777	K562	blood:	n/a	chr1:92231639-92231650
17	CEBPB	chr1:92231495-92231736	HepG2	liver:	n/a	chr1:92231639-92231650
18	CEBPD	chr1:92231510-92231917	K562	blood:	n/a	n/a
19	CEBPD	chr1:92231416-92231886	K562	blood:	n/a	n/a
20	CHD2	chr1:92230934-92231199	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr1:92230260-92230410	A549	lung:	n/a	n/a
22	CTCF	chr1:92229984-92230364	H1-hESC	embryonic stem cell:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
23	CTCF	chr1:92230114-92230301	ProgFib	skin:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
24	CTCF	chr1:92230180-92230330	Hela-S3	cervix:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
25	CTCF	chr1:92230188-92230196	GM19239	blood:	n/a	n/a
26	CTCF	chr1:92230172-92230282	Hela-S3	cervix:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
27	CTCF	chr1:92229983-92230292	H1-hESC	embryonic stem cell:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
28	CTCF	chr1:92230050-92230301	K562	blood:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
29	CTCF	chr1:92230100-92230250	WERI-Rb-1	eye:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
30	CTCF	chr1:92230060-92230210	K562	blood:	n/a	n/a
31	CTCF	chr1:92230140-92230290	HBMEC	blood vessel:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
32	CTCF	chr1:92230120-92230270	HMF	breast:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
33	CTCF	chr1:92230198-92230239	GM19239	blood:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
34	CTCF	chr1:92228360-92228560	K562	blood:	n/a	n/a
35	CTCF	chr1:92230111-92230324	K562	blood:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
36	CTCF	chr1:92230100-92230250	Caco-2	colon:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
37	CTCF	chr1:92230150-92230151	GM12891	blood:	n/a	n/a
38	CTCF	chr1:92230100-92230250	HBMEC	blood vessel:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
39	CTCF	chr1:92235180-92235353	K562	blood:	n/a	n/a
40	CTCF	chr1:92229987-92230389	K562	blood:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
41	CTCF	chr1:92230140-92230290	BE2_C	brain:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
42	CTCF	chr1:92230120-92230270	HCPEpiC	choroid plexus:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
43	CTCF	chr1:92230140-92230290	HepG2	liver:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
44	CTCF	chr1:92230120-92230270	SK-N-SH_RA	brain:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
45	CTCF	chr1:92229990-92230332	K562	blood:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
46	CTCF	chr1:92230153-92230246	GM12891	blood:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
47	CTCF	chr1:92229989-92230373	K562	blood:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
48	CTCF	chr1:92230140-92230290	HCPEpiC	choroid plexus:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
49	CTCF	chr1:92230180-92230228	Fibrobl	skin:	n/a	chr1:92230204-92230217 chr1:92230202-92230220
50	CTCF	chr1:92230053-92230283	H1-hESC	embryonic stem cell:	n/a	chr1:92230204-92230217 chr1:92230202-92230220

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:92234946-92234996	SK-N-MC	brain:	n/a
2	chr1:92234946-92234996	MCF10A-Er-Src	breast:	n/a
3	chr1:92234946-92234996	BE2_C	brain:	n/a
4	chr1:92234946-92234996	Caco-2	colon:	n/a
5	chr1:92234946-92234996	BJ	skin:	n/a
6	chr1:92234946-92234996	A549	lung:	n/a
7	chr1:92234946-92234996	HMEC	breast:	n/a
8	chr1:92234946-92234996	K562	blood:	n/a
9	chr1:92234946-92234996	MCF-7	breast:	n/a
10	chr1:92234946-92234996	HRCEpiC	kidney:	n/a
11	chr1:92234946-92234996	PrEC	prostate:	n/a
12	chr1:92234946-92234996	HL-60	blood:	n/a
13	chr1:92234946-92234996	HCM	heart:	n/a
14	chr1:92234946-92234996	LNCaP	prostate:	n/a
15	chr1:92234946-92234996	HEEpiC	esophagus:	n/a
16	chr1:92234946-92234996	AG10803	skin:	n/a
17	chr1:92234946-92234996	HRPEpiC	eye:	n/a
18	chr1:92234946-92234996	HIPEpiC	eye:	n/a
19	chr1:92234946-92234996	IMR90	lung:	fetal
20	chr1:92234946-92234996	NH-A	brain:	n/a
21	chr1:92234946-92234996	H1-hESC	embryonic stem cell:	embryo
22	chr1:92234946-92234996	T-47D	breast:	n/a
23	chr1:92234946-92234996	ovcar-3	ovarian:	n/a
24	chr1:92234946-92234996	NT2-D1	testis:	n/a
25	chr1:92234946-92234996	AG09319	gingival:	n/a
26	chr1:92234946-92234996	HCT-116	colon:	n/a
27	chr1:92234946-92234996	NHBE	bronchial:	n/a
28	chr1:92234946-92234996	GM12878	blood:	n/a
29	chr1:92234946-92234996	PANC-1	pancreas:	n/a
30	chr1:92234946-92234996	AG04450	lung:	fetal
31	chr1:92234946-92234996	Jurkat	blood:	n/a
32	chr1:92234946-92234996	AoSMC	blood vessel:	n/a
33	chr1:92234946-92234996	HPAEpiC	pulmonary alveolar:	n/a
34	chr1:92234946-92234996	GM06990	blood:	n/a
35	chr1:92234946-92234996	CMK	blood:	n/a
36	chr1:92234946-92234996	ECC-1	luminal epithelium:	n/a
37	chr1:92234946-92234996	SK-N-SH_RA	brain:	n/a
38	chr1:92234946-92234996	HCF	heart:	n/a
39	chr1:92234946-92234996	NHDF-neo	bronchial:	n/a
40	chr1:92234946-92234996	SAEC	small airway:	n/a
41	chr1:92234946-92234996	HAEpiC	amniotic membrane:	n/a
42	chr1:92234946-92234996	U87	brain:	n/a
43	chr1:92234946-92234996	GM12891	blood:	n/a
44	chr1:92234946-92234996	ProgFib	skin:	n/a
45	chr1:92234946-92234996	GM19239	blood:	n/a
46	chr1:92234946-92234996	AG04449	skin:	fetal
47	chr1:92234946-92234996	HCPEpiC	choroid plexus:	n/a
48	chr1:92234946-92234996	HRE	kidney:	n/a
49	chr1:92234946-92234996	SK-N-SH	brain:	n/a
50	chr1:92234946-92234996	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:92196718..92198594-chr1:92235219..92237131,2	K562	blood:
2	chr1:92226019..92229425-chr1:92229716..92232598,3	K562	blood:
3	chr1:92222836..92226137-chr1:92226478..92228913,3	K562	blood:
4	chr1:92217896..92221069-chr1:92227993..92231134,3	K562	blood:
5	chr1:92226383..92229371-chr1:92235062..92236732,2	K562	blood:
6	chr1:92226383..92229371-chr1:92235062..92236732,2	K562	blood:
7	chr1:92221438..92225438-chr1:92226162..92228913,3	K562	blood:
8	chr1:92232541..92234077-chr1:92245076..92247021,2	K562	blood:
9	chr1:92231081..92233303-chr1:92233328..92236066,2	K562	blood:

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

Extended variants
information (count: 300 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:300 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182241223	chr1:92227927-92227928	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs12407784	chr1:92227977-92227978	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs186471375	chr1:92228090-92228091	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs17131554	chr1:92228208-92228209	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs17131555	chr1:92228252-92228253	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs565878069	chr1:92228300-92228301	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs375676807	chr1:92228330-92228331	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs373634156	chr1:92228332-92228333	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs60189847	chr1:92228368-92228369	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs147034504	chr1:92228373-92228374	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs576276228	chr1:92228420-92228421	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs117380499	chr1:92228476-92228477	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs11334581	chr1:92228491-92228492	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs397770463	chr1:92228493-92228494	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs538357101	chr1:92228506-92228507	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs386633423	chr1:92228512-92228513	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs10874925	chr1:92228514-92228515	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs544637572	chr1:92228560-92228561	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs78234327	chr1:92228573-92228574	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs552607831	chr1:92228630-92228631	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs284182	chr1:92228645-92228646	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs542888959	chr1:92228753-92228754	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs561165639	chr1:92228770-92228771	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs531753243	chr1:92228800-92228801	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs190291906	chr1:92228829-92228830	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs564879726	chr1:92228830-92228831	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs532227198	chr1:92228953-92228954	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs80249914	chr1:92228992-92228993	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs376306431	chr1:92229038-92229039	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs370439073	chr1:92229080-92229081	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs565650144	chr1:92229151-92229152	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs182499840	chr1:92229189-92229190	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs536573750	chr1:92229191-92229192	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs34602466	chr1:92229207-92229208	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs548899838	chr1:92229250-92229251	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs187490024	chr1:92229307-92229308	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs78205714	chr1:92229385-92229386	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs537195876	chr1:92229398-92229399	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs138403172	chr1:92229480-92229481	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs578065525	chr1:92229484-92229485	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs34038846	chr1:92229494-92229495	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs192944186	chr1:92229505-92229506	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs375998425	chr1:92229642-92229643	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs369416734	chr1:92229646-92229647	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563237792	chr1:92229647-92229648	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs370098825	chr1:92229648-92229649	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576327444	chr1:92229724-92229725	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568795105	chr1:92229730-92229731	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs543700869	chr1:92229794-92229795	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565462416	chr1:92229813-92229814	Weak transcription Enhancers 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:316 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92197600-92230000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr1:92204800-92247000	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr1:92208400-92235800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr1:92211800-92235600	Weak transcription	Fetal Kidney	kidney
5	chr1:92213800-92235000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr1:92215200-92232400	Weak transcription	A549	lung
7	chr1:92216800-92241800	Weak transcription	Aorta	Aorta
8	chr1:92217200-92230200	Weak transcription	Pancreas	Pancrea
9	chr1:92217400-92232400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr1:92217600-92230200	Weak transcription	Hela-S3	cervix
11	chr1:92217800-92247800	Weak transcription	Small Intestine	intestine
12	chr1:92219400-92238200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr1:92220200-92229000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr1:92220200-92229200	Weak transcription	Osteobl	bone
15	chr1:92220400-92230000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:92220400-92234000	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr1:92220600-92255800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr1:92221000-92248000	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr1:92222200-92231000	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr1:92223200-92228000	Enhancers	Colon Smooth Muscle	Colon
21	chr1:92223400-92229400	Enhancers	Adipose Nuclei	Adipose
22	chr1:92223800-92228400	Enhancers	Right Atrium	heart
23	chr1:92223800-92232000	Enhancers	K562	blood
24	chr1:92224000-92228600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr1:92224000-92230000	Weak transcription	Lung	lung
26	chr1:92224200-92229400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr1:92224200-92230000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr1:92224200-92230000	Weak transcription	Spleen	Spleen
29	chr1:92224400-92230000	Weak transcription	Fetal Muscle Trunk	muscle
30	chr1:92224400-92242800	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr1:92224600-92229200	Weak transcription	NHLF	lung
32	chr1:92224800-92229000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr1:92224800-92234400	Weak transcription	Right Ventricle	heart
34	chr1:92225200-92230000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr1:92225200-92232000	Weak transcription	Brain Cingulate Gyrus	brain
36	chr1:92225200-92235000	Weak transcription	Brain Hippocampus Middle	brain
37	chr1:92225400-92234400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr1:92225400-92241600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr1:92225600-92228200	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr1:92225600-92230000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr1:92226000-92230600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr1:92226200-92228000	Enhancers	Fetal Lung	lung
43	chr1:92226200-92229200	Enhancers	HepG2	liver
44	chr1:92226400-92231200	Enhancers	Fetal Heart	heart
45	chr1:92226600-92236400	Weak transcription	Brain Substantia Nigra	brain
46	chr1:92226800-92228200	Enhancers	Fetal Muscle Leg	muscle
47	chr1:92226800-92230000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr1:92226800-92232000	Enhancers	Placenta	Placenta
49	chr1:92227000-92257200	Weak transcription	Fetal Intestine Small	intestine
50	chr1:92227200-92229000	Weak transcription	Skeletal Muscle Male	skeletal muscle

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