Variant report

Variant	nsv830181
Chromosome Location	chr1:72155983-72296578
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:267)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr1:72246451-72246721	GM12878	blood:	n/a	chr1:72246586-72246597 chr1:72246587-72246597
2	BATF	chr1:72246439-72246725	GM12878	blood:	n/a	chr1:72246586-72246597 chr1:72246587-72246597
3	BHLHE40	chr1:72205203-72205242	GM12878	blood:	n/a	n/a
4	CEBPB	chr1:72230419-72230782	HepG2	liver:	n/a	chr1:72230589-72230600
5	CEBPB	chr1:72290161-72290431	A549	lung:	n/a	chr1:72290286-72290297
6	CEBPB	chr1:72161508-72161870	IMR90	lung:	n/a	n/a
7	CEBPB	chr1:72290198-72290381	H1-hESC	embryonic stem cell:	n/a	chr1:72290286-72290297
8	CEBPB	chr1:72240165-72240391	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr1:72294559-72294726	HepG2	liver:	n/a	chr1:72294674-72294685
10	CEBPB	chr1:72290106-72290476	IMR90	lung:	n/a	chr1:72290286-72290297
11	CEBPB	chr1:72290139-72290394	K562	blood:	n/a	chr1:72290286-72290297
12	CEBPB	chr1:72290112-72290442	HepG2	liver:	n/a	chr1:72290286-72290297
13	CEBPB	chr1:72214678-72215002	IMR90	lung:	n/a	chr1:72214832-72214845
14	CEBPB	chr1:72230467-72230667	H1-hESC	embryonic stem cell:	n/a	chr1:72230589-72230600
15	CEBPB	chr1:72230408-72230785	IMR90	lung:	n/a	chr1:72230589-72230600
16	CEBPB	chr1:72274296-72274496	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr1:72230432-72230774	A549	lung:	n/a	chr1:72230589-72230600
18	CEBPB	chr1:72230483-72230683	Hela-S3	cervix:	n/a	chr1:72230589-72230600
19	CTCF	chr1:72187320-72187470	HMEC	breast:	n/a	n/a
20	CTCF	chr1:72219856-72219911	Fibrobl	skin:	n/a	n/a
21	CTCF	chr1:72187278-72187552	GM12878	blood:	n/a	n/a
22	CTCF	chr1:72261820-72261970	HPAF	blood vessel:	n/a	n/a
23	CTCF	chr1:72187280-72187430	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr1:72187340-72187490	HEK293	kidney:	n/a	n/a
25	CTCF	chr1:72195915-72195982	HUVEC	blood vessel:	n/a	chr1:72195921-72195939
26	CTCF	chr1:72277640-72277790	GM12875	blood:	n/a	n/a
27	CTCF	chr1:72187280-72187430	RPTEC	kidney:	n/a	n/a
28	CTCF	chr1:72187340-72187490	NHEK	skin:	n/a	n/a
29	CTCF	chr1:72187300-72187450	HL-60	blood:	n/a	n/a
30	CTCF	chr1:72277700-72277850	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr1:72279840-72279899	LNCaP	prostate:	n/a	n/a
32	CTCF	chr1:72261820-72261970	GM06990	blood:	n/a	n/a
33	CTCF	chr1:72174840-72174893	GM13976	blood:	n/a	n/a
34	CTCF	chr1:72219500-72219650	WI-38	lung:	n/a	n/a
35	CTCF	chr1:72172120-72172270	AG04450	lung:	n/a	n/a
36	CTCF	chr1:72195960-72196110	RPTEC	kidney:	n/a	n/a
37	CTCF	chr1:72187360-72187510	HPF	lung:	n/a	n/a
38	CTCF	chr1:72261840-72261990	HMEC	breast:	n/a	n/a
39	CTCF	chr1:72172060-72172210	HepG2	liver:	n/a	n/a
40	CTCF	chr1:72187320-72187470	GM12874	blood:	n/a	n/a
41	CTCF	chr1:72187320-72187470	BE2_C	brain:	n/a	n/a
42	CTCF	chr1:72187360-72187510	HRE	kidney:	n/a	n/a
43	CTCF	chr1:72172156-72172187	ProgFib	skin:	n/a	n/a
44	CTCF	chr1:72187340-72187490	HPF	lung:	n/a	n/a
45	CTCF	chr1:72187380-72187530	GM12869	blood:	n/a	n/a
46	CTCF	chr1:72261898-72261907	MCF-7	breast:	n/a	n/a
47	CTCF	chr1:72265966-72266039	GM20000	blood:	n/a	n/a
48	CTCF	chr1:72277580-72277730	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr1:72277680-72277830	HepG2	liver:	n/a	n/a
50	CTCF	chr1:72187400-72187406	HUVEC	blood vessel:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:72190606-72190656	NH-A	brain:	n/a
2	chr1:72190606-72190656	RPTEC	kidney:	n/a
3	chr1:72190606-72190656	HCM	heart:	n/a
4	chr1:72190606-72190656	HepG2	liver:	n/a
5	chr1:72190606-72190656	Hela-S3	cervix:	n/a
6	chr1:72190606-72190656	HEEpiC	esophagus:	n/a
7	chr1:72190606-72190656	SK-N-MC	brain:	n/a
8	chr1:72190606-72190656	PFSK-1	brain:	n/a
9	chr1:72190606-72190656	HRCEpiC	kidney:	n/a
10	chr1:72190606-72190656	GM12892	blood:	n/a
11	chr1:72190606-72190656	GM19239	blood:	n/a
12	chr1:72190606-72190656	HCPEpiC	choroid plexus:	n/a
13	chr1:72190606-72190656	AG10803	skin:	n/a
14	chr1:72190606-72190656	BJ	skin:	n/a
15	chr1:72190606-72190656	PrEC	prostate:	n/a
16	chr1:72190606-72190656	PANC-1	pancreas:	n/a
17	chr1:72190606-72190656	AG09309	skin:	n/a
18	chr1:72190606-72190656	SAEC	small airway:	n/a
19	chr1:72190606-72190656	HIPEpiC	eye:	n/a
20	chr1:72190606-72190656	AoSMC	blood vessel:	n/a
21	chr1:72190606-72190656	MCF10A-Er-Src	breast:	n/a
22	chr1:72190606-72190656	GM06990	blood:	n/a
23	chr1:72190606-72190656	NHBE	bronchial:	n/a
24	chr1:72190606-72190656	ProgFib	skin:	n/a
25	chr1:72190606-72190656	HCF	heart:	n/a
26	chr1:72190606-72190656	T-47D	breast:	n/a
27	chr1:72190606-72190656	HMEC	breast:	n/a
28	chr1:72190606-72190656	HRE	kidney:	n/a
29	chr1:72190606-72190656	CMK	blood:	n/a
30	chr1:72190606-72190656	IMR90	lung:	fetal
31	chr1:72190606-72190656	GM12878	blood:	n/a
32	chr1:72190606-72190656	U87	brain:	n/a
33	chr1:72190606-72190656	AG04450	lung:	fetal
34	chr1:72190606-72190656	ovcar-3	ovarian:	n/a
35	chr1:72190606-72190656	BE2_C	brain:	n/a
36	chr1:72190606-72190656	NT2-D1	testis:	n/a
37	chr1:72190606-72190656	NHDF-neo	bronchial:	n/a
38	chr1:72190606-72190656	AG04449	skin:	fetal
39	chr1:72190606-72190656	HCT-116	colon:	n/a
40	chr1:72190606-72190656	HRPEpiC	eye:	n/a
41	chr1:72190606-72190656	K562	blood:	n/a
42	chr1:72190606-72190656	NB4	blood:	n/a
43	chr1:72190606-72190656	GM12891	blood:	n/a
44	chr1:72190606-72190656	HUVEC	blood vessel:	n/a
45	chr1:72190606-72190656	Jurkat	blood:	n/a
46	chr1:72190606-72190656	Hepatocyte	liver:	n/a
47	chr1:72190606-72190656	SK-N-SH_RA	brain:	n/a
48	chr1:72190606-72190656	HEK293	kidney:	embryo
49	chr1:72190606-72190656	HNPCEpiC	eye:	n/a
50	chr1:72190606-72190656	ECC-1	luminal epithelium:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:72161617..72164423-chr1:72171650..72174212,2	MCF-7	breast:
2	chr1:72166413..72168725-chr1:72192259..72193957,2	K562	blood:
3	chr1:72210098..72212560-chr1:72216356..72218852,2	K562	blood:
4	chr1:72210098..72212560-chr1:72216356..72218852,2	K562	blood:
5	chr1:72166413..72168725-chr1:72192259..72193957,2	K562	blood:
6	chr1:72187008..72189556-chr1:72189903..72192438,2	MCF-7	breast:
7	chr1:72187008..72189556-chr1:72189903..72192438,2	MCF-7	breast:
8	chr1:72161617..72164423-chr1:72171650..72174212,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZRANB2-1	chr1:72259915-72260219	ENSG00000228853.1
2	lnc-ZRANB2-1	chr1:72263758-72263953	ENSG00000228853.1

No data

Variant related genes	Relation type
NEGR1	TF binding region
ENSG00000271618	TF binding region
NEGR1	CpG island
ENSG00000271618	CpG island

Extended variants
information (count: 3918 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:3918 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563910315	chr1:72155988-72155989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs115420676	chr1:72156006-72156007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs565994973	chr1:72156010-72156011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs12041607	chr1:72156019-72156020	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs4650118	chr1:72156080-72156081	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs187268073	chr1:72156087-72156088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs149883059	chr1:72156092-72156093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs116523019	chr1:72156094-72156095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs557132489	chr1:72156096-72156097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs75618323	chr1:72156097-72156098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545630618	chr1:72156106-72156107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565430625	chr1:72156238-72156239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs143756434	chr1:72156249-72156250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200326263	chr1:72156280-72156281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201048664	chr1:72156282-72156283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs199675654	chr1:72156283-72156284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs9793315	chr1:72156284-72156285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs71070896	chr1:72156292-72156293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138344388	chr1:72156297-72156298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs59019409	chr1:72156342-72156343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547015885	chr1:72156354-72156355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541019705	chr1:72156381-72156382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140435025	chr1:72156405-72156406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530098731	chr1:72156483-72156484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192347163	chr1:72156607-72156608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183800849	chr1:72156608-72156609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532170529	chr1:72156616-72156617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568364267	chr1:72156628-72156629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534255241	chr1:72156669-72156670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552387205	chr1:72156694-72156695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565792058	chr1:72156707-72156708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534941540	chr1:72156709-72156710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554236438	chr1:72156745-72156746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374866276	chr1:72156831-72156832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561988225	chr1:72156848-72156849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs554011396	chr1:72156893-72156894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs34363012	chr1:72156894-72156895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187970164	chr1:72156929-72156930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557091452	chr1:72156970-72156971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375728534	chr1:72156981-72156982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs144293988	chr1:72157057-72157058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373340386	chr1:72157071-72157072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs77841084	chr1:72157134-72157135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs115801036	chr1:72157149-72157150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572622545	chr1:72157168-72157169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541724977	chr1:72157188-72157189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561278934	chr1:72157227-72157228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530012468	chr1:72157274-72157275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs373068112	chr1:72157369-72157370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192314887	chr1:72157406-72157407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	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
Melanoma	17363583	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
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
body mass index	19812545	CNVD
Obesity	20935630	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72153600-72156000	Weak transcription	Brain Germinal Matrix	brain
2	chr1:72153600-72161200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr1:72155800-72156000	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr1:72156000-72156200	Enhancers	Brain Germinal Matrix	brain
5	chr1:72160800-72162600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr1:72161000-72163800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr1:72161200-72161600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr1:72161400-72161800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr1:72161400-72162000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:72163200-72165000	Enhancers	Thymus	Thymus
11	chr1:72163400-72165000	Enhancers	Dnd41	blood
12	chr1:72163600-72164800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr1:72163800-72164200	Enhancers	Primary T cells from cord blood	blood
14	chr1:72163800-72165000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr1:72164000-72165000	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr1:72165000-72167200	Weak transcription	Dnd41	blood
17	chr1:72165000-72171200	Weak transcription	Thymus	Thymus
18	chr1:72167200-72167400	Enhancers	Dnd41	blood
19	chr1:72168400-72169200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr1:72170200-72170800	Enhancers	Dnd41	blood
21	chr1:72170200-72180800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr1:72170800-72172200	Flanking Active TSS	Dnd41	blood
23	chr1:72171200-72171600	Enhancers	Thymus	Thymus
24	chr1:72171200-72173400	Enhancers	Fetal Thymus	thymus
25	chr1:72171400-72172200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:72171400-72173000	Enhancers	HSMM	muscle
27	chr1:72171600-72171800	Flanking Active TSS	Thymus	Thymus
28	chr1:72171600-72172400	Enhancers	Primary B cells from cord blood	blood
29	chr1:72171600-72172400	Enhancers	Muscle Satellite Cultured Cells	--
30	chr1:72171800-72172000	Enhancers	Thymus	Thymus
31	chr1:72172000-72172200	Flanking Active TSS	Thymus	Thymus
32	chr1:72172000-72172800	Enhancers	HSMMtube	muscle
33	chr1:72172200-72172400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr1:72172200-72172600	Enhancers	Primary hematopoietic stem cells	blood
35	chr1:72172200-72173000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr1:72172200-72173000	Enhancers	Thymus	Thymus
37	chr1:72172200-72173600	Enhancers	Dnd41	blood
38	chr1:72172400-72172800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr1:72172400-72173000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr1:72173000-72173200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr1:72174800-72178400	Weak transcription	Right Atrium	heart
42	chr1:72176800-72177000	Enhancers	K562	blood
43	chr1:72178600-72181400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr1:72180600-72181000	ZNF genes & repeats	Fetal Stomach	stomach
45	chr1:72180800-72181000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr1:72181000-72182400	Weak transcription	Fetal Stomach	stomach
47	chr1:72182400-72182600	Enhancers	Fetal Stomach	stomach
48	chr1:72183600-72184200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr1:72183800-72184000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr1:72186400-72187000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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