Variant report

Variant	esv16630
Chromosome Location	chr1:120142387-120150241
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	CEBPB	chr1:120144741-120145077	HepG2	liver:	n/a	chr1:120144889-120144900
2	CEBPB	chr1:120144888-120144965	H1-hESC	embryonic stem cell:	n/a	chr1:120144889-120144900
3	CEBPB	chr1:120142586-120142702	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr1:120144827-120145081	Hela-S3	cervix:	n/a	chr1:120144889-120144900
5	CEBPB	chr1:120144744-120145076	A549	lung:	n/a	chr1:120144889-120144900
6	CTCF	chr1:120150101-120150380	MCF-7	breast:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
7	CTCF	chr1:120150133-120150342	Fibrobl	skin:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
8	CTCF	chr1:120150134-120150401	LNCaP	prostate:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
9	CTCF	chr1:120150122-120150232	HepG2	liver:	n/a	n/a
10	CTCF	chr1:120150060-120150210	AG09309	skin:	n/a	n/a
11	CTCF	chr1:120150086-120150262	H1-hESC	embryonic stem cell:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
12	CTCF	chr1:120150140-120150363	A549	lung:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
13	CTCF	chr1:120150112-120150355	HUVEC	blood vessel:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
14	CTCF	chr1:120150135-120150298	A549	lung:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
15	CTCF	chr1:120150186-120150298	Pancreas_OC	pancreas:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
16	CTCF	chr1:120150205-120150271	Spleen_OC	spleen:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
17	CTCF	chr1:120150105-120150367	MCF-7	breast:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
18	CTCF	chr1:120150107-120150380	GM19240	blood:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
19	CTCF	chr1:120150122-120150361	ProgFib	skin:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
20	CTCF	chr1:120150107-120150392	GM19238	blood:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
21	CTCF	chr1:120150139-120150345	GM20000	blood:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
22	CTCF	chr1:120150107-120150368	MCF-7	breast:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
23	CTCF	chr1:120150060-120150210	AG09319	gingival:	n/a	n/a
24	CTCF	chr1:120150060-120150210	GM06990	blood:	n/a	n/a
25	CTCF	chr1:120149740-120149890	GM12872	blood:	n/a	n/a
26	CTCF	chr1:120150107-120150371	GM19239	blood:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
27	CTCF	chr1:120150174-120150344	Kidney_OC	kidney:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
28	CTCF	chr1:120150123-120150383	GM10266	blood:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
29	CTCF	chr1:120150100-120150537	K562	blood:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
30	CTCF	chr1:120149954-120149978	K562	blood:	n/a	n/a
31	CTCF	chr1:120150060-120150210	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr1:120150080-120150230	BE2_C	brain:	n/a	n/a
33	CTCF	chr1:120150040-120150190	BJ	skin:	n/a	n/a
34	CTCF	chr1:120150182-120150326	GM13976	blood:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
35	CTCF	chr1:120150114-120150361	HepG2	liver:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
36	CTCF	chr1:120149960-120150110	GM12872	blood:	n/a	n/a
37	CTCF	chr1:120150126-120150347	A549	lung:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
38	CTCF	chr1:120150104-120150381	GM12891	blood:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
39	CTCF	chr1:120150110-120150372	Hela-S3	cervix:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
40	CTCF	chr1:120150112-120150372	GM12892	blood:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
41	CTCF	chr1:120150164-120150370	Medullo	brain:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
42	CTCF	chr1:120150024-120150435	K562	blood:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
43	CTCF	chr1:120150112-120150383	MCF-7	breast:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
44	CTCF	chr1:120150101-120150421	K562	blood:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
45	CTCF	chr1:120150110-120150383	GM12878	blood:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
46	CTCF	chr1:120150140-120150350	GM10248	blood:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
47	CTCF	chr1:120150144-120150370	GM13977	blood:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
48	CTCF	chr1:120150097-120150393	K562	blood:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
49	CTCF	chr1:120150040-120150190	HAc	cerebellar:	n/a	n/a
50	CTCF	chr1:120150058-120150396	A549	lung:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:120143242-120143292	HMEC	breast:	n/a
2	chr1:120143242-120143292	AG09309	skin:	n/a
3	chr1:120143242-120143292	IMR90	lung:	fetal
4	chr1:120143242-120143292	AG04449	skin:	fetal
5	chr1:120143242-120143292	ovcar-3	ovarian:	n/a
6	chr1:120143242-120143292	SK-N-MC	brain:	n/a
7	chr1:120143242-120143292	T-47D	breast:	n/a
8	chr1:120143242-120143292	A549	lung:	n/a
9	chr1:120143242-120143292	HEK293	kidney:	embryo
10	chr1:120143242-120143292	HRPEpiC	eye:	n/a
11	chr1:120143242-120143292	ECC-1	luminal epithelium:	n/a
12	chr1:120143242-120143292	HUVEC	blood vessel:	n/a
13	chr1:120143242-120143292	HCF	heart:	n/a
14	chr1:120143242-120143292	SAEC	small airway:	n/a
15	chr1:120143242-120143292	SK-N-SH	brain:	n/a
16	chr1:120143242-120143292	MCF-7	breast:	n/a
17	chr1:120143242-120143292	NB4	blood:	n/a
18	chr1:120143242-120143292	RPTEC	kidney:	n/a
19	chr1:120143242-120143292	CMK	blood:	n/a
20	chr1:120143242-120143292	BJ	skin:	n/a
21	chr1:120143242-120143292	NH-A	brain:	n/a
22	chr1:120143242-120143292	HIPEpiC	eye:	n/a
23	chr1:120143242-120143292	HepG2	liver:	n/a
24	chr1:120143242-120143292	HRE	kidney:	n/a
25	chr1:120143242-120143292	Caco-2	colon:	n/a
26	chr1:120143242-120143292	AG04450	lung:	fetal
27	chr1:120143242-120143292	NHDF-neo	bronchial:	n/a
28	chr1:120143242-120143292	HEEpiC	esophagus:	n/a
29	chr1:120143242-120143292	PFSK-1	brain:	n/a
30	chr1:120143242-120143292	MCF10A-Er-Src	breast:	n/a
31	chr1:120143242-120143292	PrEC	prostate:	n/a
32	chr1:120143242-120143292	HAEpiC	amniotic membrane:	n/a
33	chr1:120143242-120143292	AG09319	gingival:	n/a
34	chr1:120143242-120143292	HCT-116	colon:	n/a
35	chr1:120143242-120143292	LNCaP	prostate:	n/a
36	chr1:120143242-120143292	PANC-1	pancreas:	n/a
37	chr1:120143242-120143292	AG10803	skin:	n/a
38	chr1:120143242-120143292	Hepatocyte	liver:	n/a
39	chr1:120143242-120143292	U87	brain:	n/a
40	chr1:120143242-120143292	HCPEpiC	choroid plexus:	n/a
41	chr1:120143242-120143292	GM06990	blood:	n/a
42	chr1:120143242-120143292	SK-N-SH_RA	brain:	n/a
43	chr1:120143242-120143292	HNPCEpiC	eye:	n/a
44	chr1:120143242-120143292	ProgFib	skin:	n/a
45	chr1:120143242-120143292	BE2_C	brain:	n/a
46	chr1:120143242-120143292	H1-hESC	embryonic stem cell:	embryo
47	chr1:120143242-120143292	HCM	heart:	n/a
48	chr1:120143242-120143292	K562	blood:	n/a
49	chr1:120143242-120143292	HL-60	blood:	n/a
50	chr1:120143242-120143292	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:120145059..120147660-chr1:120162749..120165475,2	MCF-7	breast:
2	chr1:120091982..120092921-chr1:120150180..120150935,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHGDH-1	chr1:120143780-120144107	ENSG00000242959.1
2	lnc-ZNF697-3	chr1:120148999-120149695	NONHSAT005569
3	lnc-PHGDH-1	chr1:120144910-120145118	ENSG00000242959.1

Variant related genes	Relation type
LINC00622	TF binding region
GAPDHP33	TF binding region
HSD3BP5	TF binding region
LINC00622	CpG island
GAPDHP33	CpG island
HSD3BP5	CpG island

Extended variants
information (count: 309 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183084829	chr1:120142441-120142442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs187625218	chr1:120142443-120142444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs190947276	chr1:120142446-120142447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78496464	chr1:120142451-120142452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs587770683	chr1:120142461-120142462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs587626382	chr1:120142464-120142465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376177916	chr1:120142487-120142488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs587681878	chr1:120142501-120142502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs112832031	chr1:120142509-120142510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs587630958	chr1:120142511-120142512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs149441745	chr1:120142518-120142519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs587746779	chr1:120142528-120142529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs146389108	chr1:120142550-120142551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs58222509	chr1:120142601-120142602	Weak transcription Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
15	rs12142582	chr1:120142603-120142604	Weak transcription Enhancers	TF binding region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs397703488	chr1:120142614-120142615	Weak transcription Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
17	rs11802146	chr1:120142615-120142616	Weak transcription Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
18	rs183556028	chr1:120142616-120142617	Weak transcription Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
19	rs12123068	chr1:120142626-120142627	Weak transcription Enhancers	TF binding region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs139720561	chr1:120142636-120142637	Weak transcription Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
21	rs371725355	chr1:120142665-120142666	Weak transcription Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
22	rs587671905	chr1:120142689-120142690	Weak transcription Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
23	rs367899682	chr1:120142705-120142706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs587737215	chr1:120142706-120142707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs587628875	chr1:120142718-120142719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs11437917	chr1:120142722-120142723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs587671262	chr1:120142724-120142725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs587728634	chr1:120142728-120142729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs111656104	chr1:120142739-120142740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs587626493	chr1:120142780-120142781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11590734	chr1:120142789-120142790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs587683853	chr1:120142854-120142855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192723216	chr1:120142890-120142891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs587617576	chr1:120142894-120142895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs184555965	chr1:120142904-120142905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs587753283	chr1:120142905-120142906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs113697433	chr1:120142959-120142960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs587731630	chr1:120142976-120142977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs587775355	chr1:120143076-120143077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs375451635	chr1:120143161-120143162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs587664207	chr1:120143178-120143179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs376693479	chr1:120143242-120143243	Weak transcription Enhancers	CpG island	3 gene(s)	Overlapped CNVs	n/a
43	rs77537246	chr1:120143338-120143339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs72695115	chr1:120143370-120143371	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs188341042	chr1:120143444-120143445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs587709581	chr1:120143447-120143448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs79362039	chr1:120143448-120143449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs587671327	chr1:120143465-120143466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs191953587	chr1:120143467-120143468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs74883823	chr1:120143517-120143518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Breast cancer	21364760	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
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	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	20164920	CNVD
Cancer	21272361	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:136 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:120115200-120160800	Weak transcription	Gastric	stomach
2	chr1:120133600-120144800	Weak transcription	Placenta	Placenta
3	chr1:120135200-120151000	Weak transcription	Fetal Stomach	stomach
4	chr1:120136800-120142800	Weak transcription	Fetal Intestine Small	intestine
5	chr1:120139000-120145000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr1:120139000-120145200	Weak transcription	NHEK	skin
7	chr1:120139200-120145600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:120139200-120145600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr1:120139200-120145800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr1:120139200-120146000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr1:120139400-120146000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr1:120139800-120156600	Weak transcription	Left Ventricle	heart
13	chr1:120141800-120150600	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr1:120142400-120146800	Enhancers	Fetal Lung	lung
15	chr1:120142800-120143400	Enhancers	Fetal Intestine Small	intestine
16	chr1:120142800-120146400	Enhancers	Fetal Intestine Large	intestine
17	chr1:120143400-120144400	Weak transcription	Fetal Intestine Small	intestine
18	chr1:120143800-120144200	Enhancers	Ovary	ovary
19	chr1:120144200-120145200	Weak transcription	HMEC	breast
20	chr1:120144200-120145800	Weak transcription	Ovary	ovary
21	chr1:120144400-120145200	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr1:120144400-120145400	Enhancers	Fetal Intestine Small	intestine
23	chr1:120144600-120146800	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr1:120144800-120145200	Active TSS	Placenta	Placenta
25	chr1:120144800-120145200	Enhancers	HepG2	liver
26	chr1:120144800-120145400	Weak transcription	Fetal Brain Male	brain
27	chr1:120145000-120145600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr1:120145000-120145600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr1:120145000-120146200	Enhancers	HUVEC	blood vessel
30	chr1:120145200-120145400	Flanking Active TSS	Placenta	Placenta
31	chr1:120145200-120145400	Enhancers	Lung	lung
32	chr1:120145200-120146200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
33	chr1:120145200-120146600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr1:120145200-120147000	Enhancers	HMEC	breast
35	chr1:120145200-120147600	Weak transcription	HepG2	liver
36	chr1:120145200-120148600	Enhancers	NHEK	skin
37	chr1:120145400-120145600	Enhancers	Placenta	Placenta
38	chr1:120145400-120146000	Weak transcription	Lung	lung
39	chr1:120145400-120149200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr1:120145400-120150800	Weak transcription	Fetal Intestine Small	intestine
41	chr1:120145600-120145800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr1:120145600-120145800	Flanking Active TSS	Placenta	Placenta
43	chr1:120145600-120146000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr1:120145600-120146600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr1:120145600-120146800	Enhancers	Osteobl	bone
46	chr1:120145600-120147000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr1:120145600-120149400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr1:120145800-120146200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr1:120145800-120146400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr1:120145800-120146400	Enhancers	Breast Myoepithelial Primary Cells	Breast

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