Variant report

Variant	nsv872180
Chromosome Location	chr1:120366055-120412885
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:624)
CpG islands
(count:613)
Chromatin interactive
region (count:33)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:624 , 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	chr1:120392364-120392392	K562	blood:	n/a	n/a
2	ARID3A	chr1:120402048-120402592	K562	blood:	n/a	n/a
3	ARID3A	chr1:120386952-120387123	K562	blood:	n/a	n/a
4	ATF1	chr1:120402001-120402616	K562	blood:	n/a	n/a
5	ATF1	chr1:120398236-120398340	K562	blood:	n/a	n/a
6	ATF1	chr1:120410011-120410219	K562	blood:	n/a	n/a
7	ATF1	chr1:120391966-120392057	K562	blood:	n/a	n/a
8	ATF1	chr1:120383498-120383699	K562	blood:	n/a	n/a
9	ATF3	chr1:120402162-120402649	K562	blood:	n/a	n/a
10	BACH1	chr1:120412409-120412437	K562	blood:	n/a	n/a
11	BATF	chr1:120386780-120387005	GM12878	blood:	n/a	n/a
12	BATF	chr1:120386771-120387113	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:120387330-120387656	GM12878	blood:	n/a	n/a
14	BHLHE40	chr1:120385809-120385829	K562	blood:	n/a	n/a
15	BHLHE40	chr1:120387086-120387158	K562	blood:	n/a	n/a
16	BHLHE40	chr1:120386765-120387007	HepG2	liver:	n/a	n/a
17	BHLHE40	chr1:120402075-120402625	K562	blood:	n/a	n/a
18	CBX3	chr1:120402018-120402716	K562	blood:	n/a	n/a
19	CEBPB	chr1:120408184-120408568	IMR90	lung:	n/a	n/a
20	CEBPB	chr1:120380862-120381233	HepG2	liver:	n/a	chr1:120381035-120381046 chr1:120381036-120381047 chr1:120381035-120381048
21	CEBPB	chr1:120402181-120402652	K562	blood:	n/a	n/a
22	CEBPB	chr1:120409436-120409447	IMR90	lung:	n/a	n/a
23	CEBPB	chr1:120402260-120402530	K562	blood:	n/a	n/a
24	CEBPB	chr1:120380868-120381220	K562	blood:	n/a	chr1:120381035-120381046 chr1:120381036-120381047 chr1:120381035-120381048
25	CEBPB	chr1:120412709-120412901	K562	blood:	n/a	chr1:120412787-120412798
26	CEBPB	chr1:120380857-120381208	IMR90	lung:	n/a	chr1:120381035-120381046 chr1:120381036-120381047 chr1:120381035-120381048
27	CEBPD	chr1:120383271-120383766	K562	blood:	n/a	n/a
28	CEBPD	chr1:120402145-120402665	K562	blood:	n/a	n/a
29	CEBPD	chr1:120383335-120383800	K562	blood:	n/a	n/a
30	CTCF	chr1:120369780-120369930	GM12873	blood:	n/a	chr1:120369843-120369861 chr1:120369849-120369858 chr1:120369838-120369859
31	CTCF	chr1:120369780-120369930	HPAF	blood vessel:	n/a	chr1:120369843-120369861 chr1:120369849-120369858 chr1:120369838-120369859
32	CTCF	chr1:120412822-120414436	SK-N-SH	brain:	n/a	chr1:120413710-120413726 chr1:120413709-120413727
33	CTCF	chr1:120369400-120369550	RPTEC	kidney:	n/a	n/a
34	CTCF	chr1:120387000-120387150	AG09309	skin:	n/a	n/a
35	CTCF	chr1:120386890-120387142	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr1:120369740-120369890	GM12801	blood:	n/a	chr1:120369843-120369861 chr1:120369849-120369858 chr1:120369838-120369859
37	CTCF	chr1:120369740-120369890	HMEC	breast:	n/a	chr1:120369843-120369861 chr1:120369849-120369858 chr1:120369838-120369859
38	CTCF	chr1:120386920-120387070	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr1:120369800-120369950	GM12864	blood:	n/a	chr1:120369843-120369861 chr1:120369849-120369858 chr1:120369838-120369859
40	CTCF	chr1:120369815-120369930	Fibrobl	skin:	n/a	chr1:120369843-120369861 chr1:120369849-120369858 chr1:120369838-120369859
41	CTCF	chr1:120386880-120387030	AG04450	lung:	n/a	n/a
42	CTCF	chr1:120386960-120387110	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr1:120386860-120387010	GM12867	blood:	n/a	n/a
44	CTCF	chr1:120386900-120387050	NB4	blood:	n/a	n/a
45	CTCF	chr1:120386798-120387209	A549	lung:	n/a	n/a
46	CTCF	chr1:120369820-120369970	GM12873	blood:	n/a	chr1:120369843-120369861 chr1:120369849-120369858 chr1:120369838-120369859
47	CTCF	chr1:120369940-120370090	GM12865	blood:	n/a	n/a
48	CTCF	chr1:120386940-120387090	AG09319	gingival:	n/a	n/a
49	CTCF	chr1:120369778-120369940	ProgFib	skin:	n/a	chr1:120369843-120369861 chr1:120369849-120369858 chr1:120369838-120369859
50	CTCF	chr1:120369380-120369530	HFF-Myc	foreskin:	n/a	n/a

(count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:120395943-120395993	NT2-D1	testis:	n/a
2	chr1:120394120-120394170	HCT-116	colon:	n/a
3	chr1:120389211-120389261	Hela-S3	cervix:	n/a
4	chr1:120395943-120395993	NT2-D1	testis:	n/a
5	chr1:120394120-120394170	HCT-116	colon:	n/a
6	chr1:120389211-120389261	Hela-S3	cervix:	n/a
7	chr1:120396074-120396124	RPTEC	kidney:	n/a
8	chr1:120377779-120377829	HAEpiC	amniotic membrane:	n/a
9	chr1:120387083-120387133	HPAEpiC	pulmonary alveolar:	n/a
10	chr1:120377779-120377829	Jurkat	blood:	n/a
11	chr1:120387299-120387349	HCF	heart:	n/a
12	chr1:120387083-120387133	HCPEpiC	choroid plexus:	n/a
13	chr1:120377779-120377829	K562	blood:	n/a
14	chr1:120387083-120387133	A549	lung:	n/a
15	chr1:120377779-120377829	GM12878	blood:	n/a
16	chr1:120395943-120395993	HCM	heart:	n/a
17	chr1:120395857-120395907	HCM	heart:	n/a
18	chr1:120394120-120394170	K562	blood:	n/a
19	chr1:120396167-120396217	SKMC	muscle:	n/a
20	chr1:120396167-120396217	U87	brain:	n/a
21	chr1:120377779-120377829	Hepatocyte	liver:	n/a
22	chr1:120395943-120395993	CMK	blood:	n/a
23	chr1:120396167-120396217	BE2_C	brain:	n/a
24	chr1:120395943-120395993	PANC-1	pancreas:	n/a
25	chr1:120394120-120394170	BE2_C	brain:	n/a
26	chr1:120395857-120395907	Jurkat	blood:	n/a
27	chr1:120387299-120387349	ECC-1	luminal epithelium:	n/a
28	chr1:120387965-120388015	LNCaP	prostate:	n/a
29	chr1:120396074-120396124	HMEC	breast:	n/a
30	chr1:120387965-120388015	AG09309	skin:	n/a
31	chr1:120394120-120394170	GM12878	blood:	n/a
32	chr1:120396074-120396124	HEEpiC	esophagus:	n/a
33	chr1:120387299-120387349	NHDF-neo	bronchial:	n/a
34	chr1:120396167-120396217	AG04449	skin:	fetal
35	chr1:120396074-120396124	GM12891	blood:	n/a
36	chr1:120387083-120387133	AG09319	gingival:	n/a
37	chr1:120394120-120394170	GM12891	blood:	n/a
38	chr1:120387965-120388015	HepG2	liver:	n/a
39	chr1:120395943-120395993	HEK293	kidney:	embryo
40	chr1:120394120-120394170	SAEC	small airway:	n/a
41	chr1:120396167-120396217	PANC-1	pancreas:	n/a
42	chr1:120396074-120396124	MCF10A-Er-Src	breast:	n/a
43	chr1:120395943-120395993	ProgFib	skin:	n/a
44	chr1:120394120-120394170	PANC-1	pancreas:	n/a
45	chr1:120395857-120395907	ECC-1	luminal epithelium:	n/a
46	chr1:120394120-120394170	Hela-S3	cervix:	n/a
47	chr1:120395943-120395993	A549	lung:	n/a
48	chr1:120387965-120388015	HMEC	breast:	n/a
49	chr1:120395943-120395993	HUVEC	blood vessel:	n/a
50	chr1:120387299-120387349	HMEC	breast:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:120376398..120378437-chr1:120380310..120382183,2	MCF-7	breast:
2	chr1:120401746..120405481-chr1:120411089..120413247,3	K562	blood:
3	chr1:120402638..120409843-chr1:120411143..120414879,6	K562	blood:
4	chr1:120379572..120381597-chr1:120381872..120384134,2	MCF-7	breast:
5	chr1:120407227..120409866-chr1:120411448..120413775,3	K562	blood:
6	chr1:120411363..120413507-chr1:120488348..120490535,2	MCF-7	breast:
7	chr1:120401899..120403872-chr1:120404616..120406616,2	K562	blood:
8	chr1:120396123..120397960-chr1:120398634..120401481,2	MCF-7	breast:
9	chr1:120270844..120273756-chr1:120377482..120379845,2	MCF-7	breast:
10	chr1:120395990..120398388-chr1:120402021..120403587,2	MCF-7	breast:
11	chr1:120412006..120414446-chr20:39570090..39572688,2	MCF-7	breast:
12	chr1:120376398..120378437-chr1:120380310..120382183,2	MCF-7	breast:
13	chr1:120409955..120411545-chr1:120412072..120413806,2	MCF-7	breast:
14	chr1:120400389..120402381-chr1:120411990..120414876,2	MCF-7	breast:
15	chr1:120402254..120403816-chr1:120407208..120410128,2	K562	blood:
16	chr1:120395990..120398388-chr1:120402021..120403587,2	MCF-7	breast:
17	chr1:120324664..120326745-chr1:120374346..120376019,2	MCF-7	breast:
18	chr1:120401899..120403872-chr1:120404616..120406616,2	K562	blood:
19	chr1:120370478..120372574-chr1:120394062..120395720,2	MCF-7	breast:
20	chr1:120395050..120396919-chr1:120400456..120403382,2	K562	blood:
21	chr1:120379572..120381597-chr1:120381872..120384134,2	MCF-7	breast:
22	chr1:120400389..120402381-chr1:120411990..120414876,2	MCF-7	breast:
23	chr1:120401746..120405481-chr1:120411089..120413247,3	K562	blood:
24	chr1:120286305..120287642-chr1:120412794..120414270,15	MCF-7	breast:
25	chr1:120370478..120372574-chr1:120394062..120395720,2	MCF-7	breast:
26	chr1:120400878..120403434-chr1:120429544..120432344,2	MCF-7	breast:
27	chr1:120366944..120369602-chr1:120374482..120376649,2	K562	blood:
28	chr1:120409955..120411545-chr1:120412072..120413806,2	MCF-7	breast:
29	chr1:120402638..120409843-chr1:120411143..120414879,6	K562	blood:
30	chr1:120366944..120369602-chr1:120374482..120376649,2	K562	blood:
31	chr1:120396123..120397960-chr1:120398634..120401481,2	MCF-7	breast:
32	chr1:120407227..120409866-chr1:120411448..120413775,3	K562	blood:
33	chr1:120402254..120403816-chr1:120407208..120410128,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHGDH-2	chr1:120388521-120388629	XLOC_000371
2	lnc-ADAM30-1	chr1:120390862-120391484	ENSG00000247433
3	lnc-PHGDH-2	chr1:120389145-120389383	XLOC_000371

No data

Variant related genes	Relation type
NBPF7	TF binding region
PFN1P9	TF binding region
NBPF7	CpG island
PFN1P9	CpG island
ENSG00000227205	chromatin interactions
ZDHHC2	miRNA target sites

Extended variants
information (count: 1587 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1587 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4659238	chr1:120366055-120366056	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs76806899	chr1:120366220-120366221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs587635353	chr1:120366237-120366238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs587743964	chr1:120366238-120366239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs587596766	chr1:120366276-120366277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2185608	chr1:120366283-120366284	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs587729477	chr1:120366327-120366328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs144016487	chr1:120366328-120366329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs587603900	chr1:120366333-120366334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192135568	chr1:120366341-120366342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183954502	chr1:120366351-120366352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs587596068	chr1:120366383-120366384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs587665748	chr1:120366401-120366402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187764745	chr1:120366402-120366403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs587622589	chr1:120366406-120366407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs79803392	chr1:120366443-120366444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146321980	chr1:120366445-120366446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190686106	chr1:120366452-120366453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs587686456	chr1:120366482-120366483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs587762896	chr1:120366485-120366486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs587621724	chr1:120366509-120366510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376530762	chr1:120366542-120366543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs587771662	chr1:120366555-120366556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs587672858	chr1:120366558-120366559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11802228	chr1:120366590-120366591	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs182413972	chr1:120366616-120366617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs138161665	chr1:120366618-120366619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187116974	chr1:120366641-120366642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11583595	chr1:120366693-120366694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs79182831	chr1:120366701-120366702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs587605684	chr1:120366702-120366703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs587667543	chr1:120366710-120366711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs3009195	chr1:120366712-120366713	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs7516981	chr1:120366737-120366738	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs368290002	chr1:120366743-120366744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs375851059	chr1:120366752-120366753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs370549707	chr1:120366796-120366797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs116686186	chr1:120366822-120366823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs587632014	chr1:120366879-120366880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374199340	chr1:120366914-120366915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs7551999	chr1:120366958-120366959	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs144869553	chr1:120366984-120366985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147503564	chr1:120367008-120367009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191929213	chr1:120367013-120367014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs587771962	chr1:120367019-120367020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114201969	chr1:120367102-120367103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs587703010	chr1:120367193-120367194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs113874884	chr1:120367194-120367195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs587638228	chr1:120367247-120367248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113247660	chr1:120367259-120367260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Wilms tumour	21544195	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
Glioblastoma multiforme	21080181	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Aetanephric adenomas	20802469	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Systemic lupus erythematosus	21956041	CNVD
Breast cancer	21804112	CNVD
Mental retardation	21062444	CNVD
Myelofibrosis	22110671	CNVD
Emphysema	19352772	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	21272361	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ependymoma	19289631	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:173 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:120359000-120372200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr1:120370600-120372600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr1:120371400-120371600	Enhancers	Muscle Satellite Cultured Cells	--
4	chr1:120371400-120372600	Enhancers	HSMM	muscle
5	chr1:120372000-120372400	Enhancers	HSMMtube	muscle
6	chr1:120372000-120372600	Enhancers	Fetal Intestine Large	intestine
7	chr1:120372000-120372800	Enhancers	Fetal Stomach	stomach
8	chr1:120372000-120373400	Enhancers	Fetal Muscle Leg	muscle
9	chr1:120372200-120373000	Enhancers	Brain Substantia Nigra	brain
10	chr1:120372200-120373000	Active TSS	Fetal Kidney	kidney
11	chr1:120372200-120373400	Enhancers	Brain Hippocampus Middle	brain
12	chr1:120372200-120373600	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr1:120372400-120372800	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr1:120372600-120373000	Weak transcription	HSMM	muscle
15	chr1:120372600-120373400	Enhancers	Muscle Satellite Cultured Cells	--
16	chr1:120373000-120373400	Flanking Active TSS	Fetal Kidney	kidney
17	chr1:120373000-120373400	Enhancers	HSMM	muscle
18	chr1:120373000-120377000	Weak transcription	Brain Substantia Nigra	brain
19	chr1:120373400-120374000	Active TSS	Fetal Kidney	kidney
20	chr1:120375000-120375400	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr1:120375000-120375400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr1:120375000-120375600	Enhancers	H9 Cell Line	embryonic stem cell
23	chr1:120375200-120375600	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr1:120376800-120377600	Enhancers	Brain Angular Gyrus	brain
25	chr1:120377000-120377600	Enhancers	Brain Substantia Nigra	brain
26	chr1:120377000-120377800	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr1:120377600-120378000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
28	chr1:120380800-120381400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr1:120380800-120381400	Enhancers	GM12878-XiMat	blood
30	chr1:120381800-120383400	Enhancers	Fetal Muscle Leg	muscle
31	chr1:120382800-120384400	Enhancers	K562	blood
32	chr1:120383600-120383800	Enhancers	HSMMtube	muscle
33	chr1:120384400-120386800	Weak transcription	K562	blood
34	chr1:120387000-120387200	Enhancers	K562	blood
35	chr1:120389600-120390800	Enhancers	GM12878-XiMat	blood
36	chr1:120390600-120390800	Enhancers	NHEK	skin
37	chr1:120395000-120400400	Weak transcription	Fetal Intestine Small	intestine
38	chr1:120395800-120396000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr1:120395800-120396200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr1:120396000-120402400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr1:120397800-120398000	Enhancers	K562	blood
42	chr1:120398000-120398200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr1:120398200-120398600	Enhancers	HepG2	liver
44	chr1:120398200-120400600	Weak transcription	K562	blood
45	chr1:120398600-120400600	Weak transcription	HepG2	liver
46	chr1:120398600-120400800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr1:120400200-120402400	Enhancers	Fetal Intestine Large	intestine
48	chr1:120400400-120402600	Enhancers	Fetal Intestine Small	intestine
49	chr1:120400600-120401000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr1:120400600-120401000	Enhancers	Sigmoid Colon	Sigmoid Colon

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