Variant report

Variant	esv2754874
Chromosome Location	chr1:120126990-120156051
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:418)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:418 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:120151890-120151896	K562	blood:	n/a	n/a
2	ATF3	chr1:120154165-120154614	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr1:120154276-120154532	K562	blood:	n/a	n/a
4	BHLHE40	chr1:120154235-120154668	K562	blood:	n/a	n/a
5	CEBPB	chr1:120144827-120145081	Hela-S3	cervix:	n/a	chr1:120144889-120144900
6	CEBPB	chr1:120144744-120145076	A549	lung:	n/a	chr1:120144889-120144900
7	CEBPB	chr1:120144888-120144965	H1-hESC	embryonic stem cell:	n/a	chr1:120144889-120144900
8	CEBPB	chr1:120142586-120142702	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr1:120144741-120145077	HepG2	liver:	n/a	chr1:120144889-120144900
10	CEBPB	chr1:120152171-120152183	HepG2	liver:	n/a	n/a
11	CEBPB	chr1:120154268-120154461	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr1:120152150-120152238	K562	blood:	n/a	chr1:120152213-120152224
13	CEBPB	chr1:120152140-120152301	H1-hESC	embryonic stem cell:	n/a	chr1:120152213-120152224
14	CHD2	chr1:120154302-120154481	Hela-S3	cervix:	n/a	n/a
15	CHD2	chr1:120154059-120154552	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr1:120154340-120154490	RPTEC	kidney:	n/a	chr1:120154411-120154432
17	CTCF	chr1:120150040-120150190	BJ	skin:	n/a	n/a
18	CTCF	chr1:120154299-120154510	A549	lung:	n/a	chr1:120154411-120154432
19	CTCF	chr1:120154258-120154561	GM10266	blood:	n/a	chr1:120154411-120154432
20	CTCF	chr1:120150516-120150537	HUVEC	blood vessel:	n/a	n/a
21	CTCF	chr1:120154257-120154582	Gliobla	brain:	n/a	chr1:120154411-120154432
22	CTCF	chr1:120154320-120154470	GM12867	blood:	n/a	chr1:120154411-120154432
23	CTCF	chr1:120154340-120154490	HRPEpiC	eye:	n/a	chr1:120154411-120154432
24	CTCF	chr1:120154271-120154546	MCF-7	breast:	n/a	chr1:120154411-120154432
25	CTCF	chr1:120154272-120154520	GM13976	blood:	n/a	chr1:120154411-120154432
26	CTCF	chr1:120154270-120154579	T-47D	breast:	n/a	chr1:120154411-120154432
27	CTCF	chr1:120150080-120150230	BE2_C	brain:	n/a	n/a
28	CTCF	chr1:120154300-120154450	WI-38	lung:	n/a	chr1:120154411-120154432
29	CTCF	chr1:120130255-120130277	GM20000	blood:	n/a	n/a
30	CTCF	chr1:120154320-120154470	AG09309	skin:	n/a	chr1:120154411-120154432
31	CTCF	chr1:120154340-120154490	GM12867	blood:	n/a	chr1:120154411-120154432
32	CTCF	chr1:120150040-120150190	RPTEC	kidney:	n/a	n/a
33	CTCF	chr1:120154270-120154536	GM13977	blood:	n/a	chr1:120154411-120154432
34	CTCF	chr1:120154300-120154450	HFF-Myc	foreskin:	n/a	chr1:120154411-120154432
35	CTCF	chr1:120150060-120150210	A549	lung:	n/a	n/a
36	CTCF	chr1:120153900-120154050	NB4	blood:	n/a	n/a
37	CTCF	chr1:120154340-120154490	HCT-116	colon:	n/a	chr1:120154411-120154432
38	CTCF	chr1:120150369-120150374	GM20000	blood:	n/a	n/a
39	CTCF	chr1:120150100-120150537	K562	blood:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
40	CTCF	chr1:120154300-120154527	Hela-S3	cervix:	n/a	chr1:120154411-120154432
41	CTCF	chr1:120154600-120154750	AG04449	skin:	n/a	n/a
42	CTCF	chr1:120150104-120150381	GM12891	blood:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
43	CTCF	chr1:120154277-120154540	LNCaP	prostate:	n/a	chr1:120154411-120154432
44	CTCF	chr1:120154254-120154548	K562	blood:	n/a	chr1:120154411-120154432
45	CTCF	chr1:120154275-120154536	Kidney_OC	kidney:	n/a	chr1:120154411-120154432
46	CTCF	chr1:120149400-120149550	GM12873	blood:	n/a	n/a
47	CTCF	chr1:120150060-120150210	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr1:120150123-120150383	GM10266	blood:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
49	CTCF	chr1:120154320-120154470	GM12875	blood:	n/a	chr1:120154411-120154432
50	CTCF	chr1:120154260-120154410	HCM	heart:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:120143242-120143292	PrEC	prostate:	n/a
2	chr1:120143242-120143292	PANC-1	pancreas:	n/a
3	chr1:120143242-120143292	Jurkat	blood:	n/a
4	chr1:120143242-120143292	HEEpiC	esophagus:	n/a
5	chr1:120143242-120143292	HRCEpiC	kidney:	n/a
6	chr1:120143242-120143292	H1-hESC	embryonic stem cell:	embryo
7	chr1:120143242-120143292	MCF-7	breast:	n/a
8	chr1:120143242-120143292	HCPEpiC	choroid plexus:	n/a
9	chr1:120143242-120143292	GM19239	blood:	n/a
10	chr1:120143242-120143292	ProgFib	skin:	n/a
11	chr1:120143242-120143292	Caco-2	colon:	n/a
12	chr1:120143242-120143292	HUVEC	blood vessel:	n/a
13	chr1:120143242-120143292	CMK	blood:	n/a
14	chr1:120143242-120143292	SAEC	small airway:	n/a
15	chr1:120143242-120143292	RPTEC	kidney:	n/a
16	chr1:120143242-120143292	A549	lung:	n/a
17	chr1:120143242-120143292	NHDF-neo	bronchial:	n/a
18	chr1:120143242-120143292	BJ	skin:	n/a
19	chr1:120143242-120143292	HEK293	kidney:	embryo
20	chr1:120143242-120143292	HNPCEpiC	eye:	n/a
21	chr1:120143242-120143292	HAEpiC	amniotic membrane:	n/a
22	chr1:120143242-120143292	AoSMC	blood vessel:	n/a
23	chr1:120143242-120143292	HCT-116	colon:	n/a
24	chr1:120143242-120143292	HIPEpiC	eye:	n/a
25	chr1:120143242-120143292	HCF	heart:	n/a
26	chr1:120143242-120143292	Hela-S3	cervix:	n/a
27	chr1:120143242-120143292	AG04449	skin:	fetal
28	chr1:120143242-120143292	U87	brain:	n/a
29	chr1:120143242-120143292	GM06990	blood:	n/a
30	chr1:120143242-120143292	Hepatocyte	liver:	n/a
31	chr1:120143242-120143292	NH-A	brain:	n/a
32	chr1:120143242-120143292	HCM	heart:	n/a
33	chr1:120143242-120143292	HMEC	breast:	n/a
34	chr1:120143242-120143292	AG09319	gingival:	n/a
35	chr1:120143242-120143292	BE2_C	brain:	n/a
36	chr1:120143242-120143292	K562	blood:	n/a
37	chr1:120143242-120143292	SKMC	muscle:	n/a
38	chr1:120143242-120143292	T-47D	breast:	n/a
39	chr1:120143242-120143292	ovcar-3	ovarian:	n/a
40	chr1:120143242-120143292	AG10803	skin:	n/a
41	chr1:120143242-120143292	PFSK-1	brain:	n/a
42	chr1:120143242-120143292	GM12878	blood:	n/a
43	chr1:120143242-120143292	AG04450	lung:	fetal
44	chr1:120143242-120143292	MCF10A-Er-Src	breast:	n/a
45	chr1:120143242-120143292	IMR90	lung:	fetal
46	chr1:120143242-120143292	SK-N-SH_RA	brain:	n/a
47	chr1:120143242-120143292	HRE	kidney:	n/a
48	chr1:120143242-120143292	NT2-D1	testis:	n/a
49	chr1:120143242-120143292	HepG2	liver:	n/a
50	chr1:120143242-120143292	GM12892	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:120151431..120154337-chr1:120190081..120192940,2	MCF-7	breast:
2	chr1:120155133..120157085-chr1:120217009..120218744,10	K562	blood:
3	chr1:120154067..120155007-chr1:120217498..120218673,7	MCF-7	breast:
4	chr1:119914912..119915700-chr1:120154301..120154847,3	MCF-7	breast:
5	chr1:120145059..120147660-chr1:120162749..120165475,2	MCF-7	breast:
6	chr1:120125219..120126121-chr1:120153919..120154547,2	MCF-7	breast:
7	chr1:120153476..120155640-chr1:120190161..120192811,2	K562	blood:
8	chr1:120154194..120154867-chr1:120205886..120206437,3	MCF-7	breast:
9	chr1:120154003..120154965-chr1:120217033..120218809,10	K562	blood:
10	chr1:120091982..120092921-chr1:120150180..120150935,3	MCF-7	breast:
11	chr1:120153709..120155634-chr1:120202418..120204087,2	MCF-7	breast:
12	chr1:120154324..120155309-chr1:120205532..120206464,6	MCF-7	breast:
13	chr1:120154731..120156704-chr1:120158612..120160451,2	MCF-7	breast:
14	chr1:120154024..120154620-chr1:120217678..120218364,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHGDH-1	chr1:120144910-120145118	ENSG00000242959.1
2	lnc-ZNF697-3	chr1:120148999-120149695	NONHSAT005569
3	lnc-ZNF697-1	chr1:120140325-120141914	NONHSAT005570
4	lnc-ZNF697-1	chr1:120140325-120141894	ENSG00000260941.1
5	lnc-PHGDH-1	chr1:120143780-120144107	ENSG00000242959.1

No data

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
ENSG00000143067	chromatin interactions
ENSG00000092621	chromatin interactions

Extended variants
information (count: 1265 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1265 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9919159	chr1:120126990-120126991	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs114368630	chr1:120127001-120127002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145897131	chr1:120127005-120127006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs138499912	chr1:120127033-120127034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs587602711	chr1:120127166-120127167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs587638176	chr1:120127207-120127208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs587711761	chr1:120127282-120127283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs35251952	chr1:120127317-120127318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs187090124	chr1:120127326-120127327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs149262985	chr1:120127342-120127343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs587716222	chr1:120127360-120127361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs371357303	chr1:120127368-120127369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs191937528	chr1:120127374-120127375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs34900525	chr1:120127377-120127378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs587661630	chr1:120127382-120127383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs587745751	chr1:120127412-120127413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs143451284	chr1:120127446-120127447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs587676195	chr1:120127448-120127449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184278072	chr1:120127477-120127478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs374140457	chr1:120127491-120127492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs4659014	chr1:120127497-120127498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs587771877	chr1:120127529-120127530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs587628168	chr1:120127563-120127564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs587679066	chr1:120127572-120127573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs587763203	chr1:120127578-120127579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs587629088	chr1:120127642-120127643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs587716277	chr1:120127661-120127662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189039748	chr1:120127721-120127722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs147503219	chr1:120127742-120127743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs72469593	chr1:120127759-120127760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs587607038	chr1:120127761-120127762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374002670	chr1:120127765-120127766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs587717994	chr1:120127769-120127770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs368715226	chr1:120127794-120127795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs79260100	chr1:120127803-120127804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs35794584	chr1:120127804-120127805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs10923867	chr1:120127818-120127819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs587637861	chr1:120127821-120127822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs587693019	chr1:120127824-120127825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs587751949	chr1:120127839-120127840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs182377295	chr1:120127843-120127844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs368178534	chr1:120127858-120127859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10802117	chr1:120127864-120127865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373820899	chr1:120127885-120127886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs587754945	chr1:120127888-120127889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs185703792	chr1:120127938-120127939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs587703913	chr1:120127948-120127949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs587761882	chr1:120127951-120127952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs587656934	chr1:120127956-120127957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs587714279	chr1:120127972-120127973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:352 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:120111800-120129800	Weak transcription	Left Ventricle	heart
2	chr1:120112000-120129600	Weak transcription	Right Atrium	heart
3	chr1:120115200-120160800	Weak transcription	Gastric	stomach
4	chr1:120117000-120128200	Weak transcription	Placenta	Placenta
5	chr1:120117000-120128600	Weak transcription	Spleen	Spleen
6	chr1:120122000-120129000	Weak transcription	Ovary	ovary
7	chr1:120123800-120128200	Weak transcription	Fetal Intestine Small	intestine
8	chr1:120125400-120128200	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr1:120126000-120128000	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr1:120126400-120130000	Weak transcription	Fetal Lung	lung
11	chr1:120126800-120127200	Weak transcription	Fetal Muscle Leg	muscle
12	chr1:120127200-120127400	Enhancers	Fetal Muscle Leg	muscle
13	chr1:120127400-120128600	Weak transcription	Fetal Muscle Leg	muscle
14	chr1:120128000-120129000	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr1:120128000-120129000	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr1:120128200-120128400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
17	chr1:120128200-120128800	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr1:120128200-120128800	Enhancers	Placenta	Placenta
19	chr1:120128200-120129000	Enhancers	Duodenum Mucosa	Duodenum
20	chr1:120128200-120129000	Enhancers	Fetal Intestine Small	intestine
21	chr1:120128200-120131000	Enhancers	Fetal Intestine Large	intestine
22	chr1:120128400-120128600	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr1:120128600-120128800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr1:120128600-120128800	Enhancers	Fetal Muscle Leg	muscle
25	chr1:120128600-120128800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
26	chr1:120128600-120129400	Enhancers	Spleen	Spleen
27	chr1:120128800-120129000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr1:120128800-120129200	Enhancers	Fetal Kidney	kidney
29	chr1:120128800-120129200	Weak transcription	Fetal Muscle Leg	muscle
30	chr1:120128800-120129600	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr1:120128800-120129800	Weak transcription	Placenta	Placenta
32	chr1:120129000-120129400	Bivalent Enhancer	HSMM	muscle
33	chr1:120129000-120129600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr1:120129000-120129600	Enhancers	Lung	lung
35	chr1:120129000-120130200	Enhancers	Ovary	ovary
36	chr1:120129000-120131000	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr1:120129000-120132600	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr1:120129000-120132800	Weak transcription	Fetal Intestine Small	intestine
39	chr1:120129200-120129400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr1:120129200-120129600	Weak transcription	Fetal Kidney	kidney
41	chr1:120129200-120131000	Enhancers	HSMMtube	muscle
42	chr1:120129200-120131200	Enhancers	Fetal Muscle Leg	muscle
43	chr1:120129200-120133200	Weak transcription	Adipose Nuclei	Adipose
44	chr1:120129400-120130000	Weak transcription	Spleen	Spleen
45	chr1:120129400-120130800	Enhancers	HSMM	muscle
46	chr1:120129600-120130000	Weak transcription	Lung	lung
47	chr1:120129600-120130200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr1:120129600-120130200	Enhancers	Fetal Kidney	kidney
49	chr1:120129600-120130600	Enhancers	Muscle Satellite Cultured Cells	--
50	chr1:120129600-120130600	Enhancers	Right Atrium	heart

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