Variant report

Variant	nsv546821
Chromosome Location	chr1:92525678-92650349
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:633)
CpG islands
(count:979)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:633 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:92545717-92545724	K562	blood:	n/a	n/a
2	ARID3A	chr1:92545681-92545684	HepG2	liver:	n/a	n/a
3	ATF1	chr1:92608669-92608727	K562	blood:	n/a	n/a
4	ATF1	chr1:92591884-92591960	K562	blood:	n/a	n/a
5	ATF1	chr1:92530637-92530857	K562	blood:	n/a	n/a
6	BHLHE40	chr1:92545583-92546606	K562	blood:	n/a	n/a
7	BRCA1	chr1:92548328-92548357	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr1:92551261-92551662	HCT-116	colon:	n/a	n/a
9	CBX3	chr1:92545636-92546410	K562	blood:	n/a	n/a
10	CBX3	chr1:92551214-92551741	K562	blood:	n/a	n/a
11	CBX3	chr1:92551278-92551743	HCT-116	colon:	n/a	n/a
12	CBX3	chr1:92620422-92620917	HCT-116	colon:	n/a	n/a
13	CBX3	chr1:92620575-92620818	HCT-116	colon:	n/a	n/a
14	CBX3	chr1:92551256-92551644	K562	blood:	n/a	n/a
15	CCNT2	chr1:92629723-92629923	K562	blood:	n/a	n/a
16	CCNT2	chr1:92545770-92546292	K562	blood:	n/a	chr1:92545783-92545792
17	CEBPB	chr1:92644880-92645067	K562	blood:	n/a	chr1:92644942-92644955 chr1:92644942-92644955 chr1:92644942-92644955 chr1:92644944-92644955 chr1:92644944-92644955
18	CEBPB	chr1:92557000-92557575	K562	blood:	n/a	n/a
19	CEBPB	chr1:92562009-92562326	HepG2	liver:	n/a	chr1:92562163-92562174
20	CEBPB	chr1:92628358-92628558	IMR90	lung:	n/a	n/a
21	CEBPB	chr1:92561467-92561769	A549	lung:	n/a	n/a
22	CEBPB	chr1:92561627-92561711	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr1:92639841-92640073	HepG2	liver:	n/a	chr1:92640001-92640012
24	CEBPB	chr1:92647135-92647407	HepG2	liver:	n/a	chr1:92647255-92647266
25	CEBPB	chr1:92553062-92553344	IMR90	lung:	n/a	chr1:92553294-92553302
26	CEBPB	chr1:92557199-92557564	HepG2	liver:	n/a	n/a
27	CEBPB	chr1:92573101-92573256	HepG2	liver:	n/a	chr1:92573212-92573223
28	CEBPB	chr1:92557278-92557455	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr1:92650199-92650774	IMR90	lung:	n/a	n/a
30	CEBPB	chr1:92562014-92562256	Hela-S3	cervix:	n/a	chr1:92562163-92562174
31	CEBPB	chr1:92561500-92561678	K562	blood:	n/a	n/a
32	CEBPB	chr1:92557103-92557548	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr1:92637818-92637974	A549	lung:	n/a	n/a
34	CEBPB	chr1:92557218-92557555	IMR90	lung:	n/a	n/a
35	CEBPB	chr1:92561461-92561809	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr1:92557276-92557559	A549	lung:	n/a	n/a
37	CEBPB	chr1:92557333-92557513	K562	blood:	n/a	n/a
38	CEBPB	chr1:92561470-92562295	IMR90	lung:	n/a	chr1:92562163-92562174
39	CEBPB	chr1:92561447-92561785	HepG2	liver:	n/a	n/a
40	CEBPB	chr1:92628299-92628572	HepG2	liver:	n/a	n/a
41	CEBPB	chr1:92557011-92557465	K562	blood:	n/a	n/a
42	CEBPB	chr1:92557051-92557259	K562	blood:	n/a	n/a
43	CHD1	chr1:92545473-92545874	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr1:92546206-92546662	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr1:92545865-92546001	HepG2	liver:	n/a	n/a
46	CHD2	chr1:92545687-92546741	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr1:92545679-92546388	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr1:92545954-92546264	K562	blood:	n/a	n/a
49	CREB1	chr1:92545684-92546311	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr1:92545783-92546147	A549	lung:	n/a	n/a

(count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:92546040-92546090	SAEC	small airway:	n/a
2	chr1:92546040-92546090	HepG2	liver:	n/a
3	chr1:92545898-92545948	HAEpiC	amniotic membrane:	n/a
4	chr1:92546040-92546090	SAEC	small airway:	n/a
5	chr1:92546040-92546090	HepG2	liver:	n/a
6	chr1:92545898-92545948	HAEpiC	amniotic membrane:	n/a
7	chr1:92549234-92549284	PrEC	prostate:	n/a
8	chr1:92545898-92545948	Caco-2	colon:	n/a
9	chr1:92545898-92545948	IMR90	lung:	fetal
10	chr1:92546479-92546529	ProgFib	skin:	n/a
11	chr1:92546447-92546497	K562	blood:	n/a
12	chr1:92545224-92545274	HIPEpiC	eye:	n/a
13	chr1:92545650-92545700	NB4	blood:	n/a
14	chr1:92545188-92545238	AG09319	gingival:	n/a
15	chr1:92546447-92546497	AoSMC	blood vessel:	n/a
16	chr1:92545898-92545948	HRE	kidney:	n/a
17	chr1:92545580-92545630	HRPEpiC	eye:	n/a
18	chr1:92545224-92545274	NB4	blood:	n/a
19	chr1:92545888-92545938	Hepatocyte	liver:	n/a
20	chr1:92546470-92546520	HCF	heart:	n/a
21	chr1:92545580-92545630	NT2-D1	testis:	n/a
22	chr1:92545888-92545938	PANC-1	pancreas:	n/a
23	chr1:92546447-92546497	HIPEpiC	eye:	n/a
24	chr1:92545662-92545712	HL-60	blood:	n/a
25	chr1:92546479-92546529	NB4	blood:	n/a
26	chr1:92545650-92545700	NHDF-neo	bronchial:	n/a
27	chr1:92546447-92546497	BE2_C	brain:	n/a
28	chr1:92542467-92542517	NT2-D1	testis:	n/a
29	chr1:92545898-92545948	HNPCEpiC	eye:	n/a
30	chr1:92546135-92546185	SK-N-MC	brain:	n/a
31	chr1:92545768-92545818	PANC-1	pancreas:	n/a
32	chr1:92546040-92546090	HPAEpiC	pulmonary alveolar:	n/a
33	chr1:92545650-92545700	HRCEpiC	kidney:	n/a
34	chr1:92546135-92546185	SAEC	small airway:	n/a
35	chr1:92545888-92545938	MCF-7	breast:	n/a
36	chr1:92545888-92545938	SK-N-MC	brain:	n/a
37	chr1:92631249-92631299	Jurkat	blood:	n/a
38	chr1:92542467-92542517	HCF	heart:	n/a
39	chr1:92545580-92545630	HCT-116	colon:	n/a
40	chr1:92549234-92549284	ECC-1	luminal epithelium:	n/a
41	chr1:92546479-92546529	Jurkat	blood:	n/a
42	chr1:92545650-92545700	AG09319	gingival:	n/a
43	chr1:92545662-92545712	HRCEpiC	kidney:	n/a
44	chr1:92546040-92546090	HCPEpiC	choroid plexus:	n/a
45	chr1:92545580-92545630	GM12891	blood:	n/a
46	chr1:92546447-92546497	CMK	blood:	n/a
47	chr1:92546135-92546185	PrEC	prostate:	n/a
48	chr1:92545888-92545938	MCF10A-Er-Src	breast:	n/a
49	chr1:92546447-92546497	NHDF-neo	bronchial:	n/a
50	chr1:92545768-92545818	MCF10A-Er-Src	breast:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:92532650..92534894-chr1:92538818..92540475,2	K562	blood:
2	chr1:92624229..92626147-chr1:92633625..92636572,2	K562	blood:
3	chr1:92544652..92546280-chr1:92558053..92559585,2	K562	blood:
4	chr1:92556197..92558083-chr1:92563000..92565811,2	MCF-7	breast:
5	chr1:92535153..92538093-chr1:92546590..92548474,2	K562	blood:
6	chr1:92597223..92599261-chr1:92601215..92603024,2	K562	blood:
7	chr1:92529998..92532866-chr1:92545519..92547678,2	MCF-7	breast:
8	chr1:92542913..92545844-chr1:92825979..92827706,2	K562	blood:
9	chr1:92535153..92538093-chr1:92546590..92548474,2	K562	blood:
10	chr1:92641813..92643344-chr1:92644276..92646156,2	MCF-7	breast:
11	chr1:92640592..92643432-chr1:92648038..92650855,3	K562	blood:
12	chr1:92641813..92643344-chr1:92644276..92646156,2	MCF-7	breast:
13	chr1:92529291..92531947-chr1:92544374..92546080,2	K562	blood:
14	chr1:92624229..92626147-chr1:92633625..92636572,2	K562	blood:
15	chr1:92597223..92599261-chr1:92601215..92603024,2	K562	blood:
16	chr1:92628189..92630728-chr1:92634090..92636512,2	K562	blood:
17	chr1:92636751..92638708-chr14:23652231..23655007,2	MCF-7	breast:
18	chr1:91966529..91968334-chr1:92639534..92641055,2	K562	blood:
19	chr1:92545812..92549091-chr1:92549918..92553923,4	K562	blood:
20	chr1:92531679..92534472-chr1:92536505..92538325,2	K562	blood:
21	chr1:92529291..92531947-chr1:92544374..92546080,2	K562	blood:
22	chr1:91965368..91967670-chr1:92645246..92647453,2	K562	blood:
23	chr1:92628189..92630728-chr1:92634090..92636512,2	K562	blood:
24	chr1:92494787..92497358-chr1:92544717..92548251,3	MCF-7	breast:
25	chr1:92529998..92532866-chr1:92545519..92547678,2	MCF-7	breast:
26	chr1:92532650..92534894-chr1:92538818..92540475,2	K562	blood:
27	chr1:92556197..92558083-chr1:92563000..92565811,2	MCF-7	breast:
28	chr1:92640592..92643432-chr1:92648038..92650855,3	K562	blood:

No data

Variant related genes	Relation type
KIAA1107	TF binding region
LPCAT2BP	TF binding region
GAPDHP46	TF binding region
BTBD8	TF binding region
SETSIP	TF binding region
ENSG00000273487	TF binding region
PRKAR1AP	TF binding region
KIAA1107	CpG island
LPCAT2BP	CpG island
GAPDHP46	CpG island
BTBD8	CpG island
SETSIP	CpG island
ENSG00000273487	CpG island
PRKAR1AP	CpG island
ENSG00000097046	chromatin interactions
ENSG00000233228	chromatin interactions
ENSG00000092068	chromatin interactions
ENSG00000172031	chromatin interactions
ENSG00000189195	chromatin interactions
ENSG00000215277	chromatin interactions

Extended variants
information (count: 4238 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:4238 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6668529	chr1:92525678-92525679	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531789674	chr1:92525697-92525698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563608568	chr1:92525776-92525777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs549601001	chr1:92525799-92525800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs6683065	chr1:92525809-92525810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546024506	chr1:92525810-92525811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs77524909	chr1:92525819-92525820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115957883	chr1:92525983-92525984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs78480155	chr1:92525988-92525989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528256811	chr1:92525990-92525991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs79331797	chr1:92525998-92525999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111746173	chr1:92525999-92526000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs193027705	chr1:92526000-92526001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs77181457	chr1:92526119-92526120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530128891	chr1:92526166-92526167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs140171410	chr1:92526167-92526168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146993283	chr1:92526185-92526186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76527221	chr1:92526198-92526199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs559139040	chr1:92526293-92526294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570970516	chr1:92526334-92526335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559957497	chr1:92526366-92526367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs74883103	chr1:92526422-92526423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574153909	chr1:92526439-92526440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574421107	chr1:92526443-92526444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541465582	chr1:92526526-92526527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs147613018	chr1:92526532-92526533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575521947	chr1:92526547-92526548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545796255	chr1:92526583-92526584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564379423	chr1:92526598-92526599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374897844	chr1:92526645-92526646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374297334	chr1:92526699-92526700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372076141	chr1:92526710-92526711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577645796	chr1:92526728-92526729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs116306956	chr1:92526738-92526739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs74328305	chr1:92526748-92526749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185710264	chr1:92526774-92526775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs11166042	chr1:92526777-92526778	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs12728005	chr1:92526904-92526905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570452843	chr1:92526955-92526956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569937159	chr1:92527043-92527044	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs146069837	chr1:92527142-92527143	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs552614534	chr1:92527152-92527153	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs571075801	chr1:92527289-92527290	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs189035514	chr1:92527295-92527296	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs192424265	chr1:92527303-92527304	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs183569809	chr1:92527329-92527330	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs138153902	chr1:92527330-92527331	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs74102814	chr1:92527337-92527338	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs149553765	chr1:92527366-92527367	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs556985676	chr1:92527391-92527392	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

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

Chromatin state (count:1194 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92497800-92534200	Weak transcription	Dnd41	blood
2	chr1:92512200-92527200	Weak transcription	Brain Angular Gyrus	brain
3	chr1:92516800-92536200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr1:92531800-92532000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr1:92531800-92532600	Enhancers	Pancreas	Pancrea
6	chr1:92534600-92535200	Enhancers	A549	lung
7	chr1:92534800-92535200	Enhancers	K562	blood
8	chr1:92536200-92536600	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr1:92536200-92536600	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr1:92540800-92545400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr1:92542800-92545400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr1:92545000-92545200	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr1:92545000-92545200	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr1:92545000-92545200	Weak transcription	Dnd41	blood
15	chr1:92545000-92545400	Enhancers	Fetal Muscle Trunk	muscle
16	chr1:92545200-92545400	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr1:92545200-92545400	Enhancers	Primary B cells from cord blood	blood
18	chr1:92545200-92545400	Enhancers	Primary T cells fromperipheralblood	blood
19	chr1:92545200-92545400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr1:92545200-92545400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
21	chr1:92545200-92545400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr1:92545200-92545400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr1:92545200-92545400	Enhancers	Muscle Satellite Cultured Cells	--
24	chr1:92545200-92545400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr1:92545200-92545400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:92545200-92545400	Enhancers	Adipose Nuclei	Adipose
27	chr1:92545200-92545400	Enhancers	Liver	Liver
28	chr1:92545200-92545400	Enhancers	Brain Angular Gyrus	brain
29	chr1:92545200-92545400	Enhancers	Duodenum Mucosa	Duodenum
30	chr1:92545200-92545400	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr1:92545200-92545400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr1:92545200-92545400	Active TSS	Fetal Heart	heart
33	chr1:92545200-92545400	Enhancers	Fetal Lung	lung
34	chr1:92545200-92545400	Enhancers	Fetal Thymus	thymus
35	chr1:92545200-92545400	Enhancers	Rectal Smooth Muscle	rectum
36	chr1:92545200-92545400	Enhancers	Skeletal Muscle Male	skeletal muscle
37	chr1:92545200-92545400	Enhancers	Stomach Mucosa	stomach
38	chr1:92545200-92545400	Enhancers	Dnd41	blood
39	chr1:92545200-92545400	Enhancers	HMEC	breast
40	chr1:92545200-92545400	Active TSS	Monocytes-CD14+_RO01746	blood
41	chr1:92545200-92545400	Enhancers	NH-A	brain
42	chr1:92545200-92545400	Enhancers	NHLF	lung
43	chr1:92545200-92545600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
44	chr1:92545200-92545600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
45	chr1:92545200-92545800	Active TSS	Fetal Brain Female	brain
46	chr1:92545200-92546000	Active TSS	Brain Germinal Matrix	brain
47	chr1:92545200-92546800	Active TSS	ES-I3 Cell Line	embryonic stem cell
48	chr1:92545200-92546800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr1:92545200-92546800	Active TSS	HUES6 Cell Line	embryonic stem cell
50	chr1:92545200-92546800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell

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