Variant report

Variant	nsv546307
Chromosome Location	chr1:58707111-58733050
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:388)
CpG islands
(count:1159)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:388 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:58716043-58716449	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr1:58715990-58716418	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:58715404-58716410	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr1:58714319-58714549	GM12878	blood:	n/a	n/a
5	BCL3	chr1:58712076-58712761	GM12878	blood:	n/a	n/a
6	BCL3	chr1:58712158-58712677	GM12878	blood:	n/a	n/a
7	CEBPB	chr1:58726621-58726706	HepG2	liver:	n/a	chr1:58726655-58726666
8	CEBPB	chr1:58716094-58716313	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:58727254-58727400	HepG2	liver:	n/a	chr1:58727327-58727340 chr1:58727329-58727340 chr1:58727329-58727340 chr1:58727327-58727340 chr1:58727327-58727338
10	CEBPB	chr1:58716163-58716330	HepG2	liver:	n/a	n/a
11	CEBPB	chr1:58716087-58716404	K562	blood:	n/a	n/a
12	CEBPB	chr1:58716094-58716372	K562	blood:	n/a	n/a
13	CEBPB	chr1:58726057-58726249	HepG2	liver:	n/a	chr1:58726184-58726195 chr1:58726186-58726197
14	CEBPB	chr1:58715984-58716420	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr1:58726585-58726811	A549	lung:	n/a	chr1:58726655-58726666
16	CHD2	chr1:58715956-58716418	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTBP2	chr1:58715231-58716476	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr1:58717336-58717662	IMR90	lung:	n/a	n/a
19	CTCF	chr1:58717310-58717691	K562	blood:	n/a	n/a
20	CTCF	chr1:58717440-58717590	AoAF	blood vessel:	n/a	n/a
21	CTCF	chr1:58717420-58717570	AG09309	skin:	n/a	n/a
22	CTCF	chr1:58717411-58717627	Gliobla	brain:	n/a	n/a
23	CTCF	chr1:58716240-58716390	GM12864	blood:	n/a	n/a
24	CTCF	chr1:58717400-58717550	NB4	blood:	n/a	n/a
25	CTCF	chr1:58717300-58717450	AG04450	lung:	n/a	n/a
26	CTCF	chr1:58717400-58717550	HRE	kidney:	n/a	n/a
27	CTCF	chr1:58717460-58717610	HUVEC	blood vessel:	n/a	n/a
28	CTCF	chr1:58716073-58716363	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr1:58717452-58717621	GM19238	blood:	n/a	n/a
30	CTCF	chr1:58717400-58717550	GM12867	blood:	n/a	n/a
31	CTCF	chr1:58717440-58717590	HPAF	blood vessel:	n/a	n/a
32	CTCF	chr1:58716160-58716310	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr1:58717380-58717530	GM12870	blood:	n/a	n/a
34	CTCF	chr1:58717431-58717604	ProgFib	skin:	n/a	n/a
35	CTCF	chr1:58717400-58717550	HepG2	liver:	n/a	n/a
36	CTCF	chr1:58717460-58717610	GM12871	blood:	n/a	n/a
37	CTCF	chr1:58717380-58717530	HRE	kidney:	n/a	n/a
38	CTCF	chr1:58716120-58716270	BJ	skin:	n/a	n/a
39	CTCF	chr1:58716260-58716410	GM12875	blood:	n/a	n/a
40	CTCF	chr1:58717360-58717510	HFF-Myc	foreskin:	n/a	n/a
41	CTCF	chr1:58715558-58715669	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr1:58715880-58716030	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr1:58715600-58715750	AG04449	skin:	n/a	n/a
44	CTCF	chr1:58717428-58717599	MCF-7	breast:	n/a	n/a
45	CTCF	chr1:58715760-58715910	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr1:58716120-58716270	RPTEC	kidney:	n/a	n/a
47	CTCF	chr1:58717400-58717550	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr1:58717460-58717610	GM12875	blood:	n/a	n/a
49	CTCF	chr1:58717420-58717570	GM12869	blood:	n/a	n/a
50	CTCF	chr1:58716160-58716310	HRPEpiC	eye:	n/a	n/a

(count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:58716662-58716712	SAEC	small airway:	n/a
2	chr1:58715499-58715549	AG09319	gingival:	n/a
3	chr1:58713941-58713991	T-47D	breast:	n/a
4	chr1:58716033-58716083	RPTEC	kidney:	n/a
5	chr1:58716018-58716068	ECC-1	luminal epithelium:	n/a
6	chr1:58713367-58713417	SK-N-MC	brain:	n/a
7	chr1:58716377-58716427	T-47D	breast:	n/a
8	chr1:58714305-58714355	HCM	heart:	n/a
9	chr1:58715744-58715794	HCT-116	colon:	n/a
10	chr1:58717632-58717682	NHDF-neo	bronchial:	n/a
11	chr1:58716306-58716356	SK-N-MC	brain:	n/a
12	chr1:58715539-58715589	AG04449	skin:	fetal
13	chr1:58716018-58716068	GM12878	blood:	n/a
14	chr1:58715539-58715589	PrEC	prostate:	n/a
15	chr1:58716306-58716356	SK-N-SH	brain:	n/a
16	chr1:58714305-58714355	MCF-7	breast:	n/a
17	chr1:58714305-58714355	HepG2	liver:	n/a
18	chr1:58714452-58714502	AG09319	gingival:	n/a
19	chr1:58717632-58717682	A549	lung:	n/a
20	chr1:58712062-58712112	HCM	heart:	n/a
21	chr1:58715499-58715549	Hepatocyte	liver:	n/a
22	chr1:58715553-58715603	HRCEpiC	kidney:	n/a
23	chr1:58714305-58714355	SK-N-SH	brain:	n/a
24	chr1:58716662-58716712	HEK293	kidney:	embryo
25	chr1:58716662-58716712	NT2-D1	testis:	n/a
26	chr1:58717632-58717682	GM12891	blood:	n/a
27	chr1:58715539-58715589	MCF-7	breast:	n/a
28	chr1:58716257-58716307	GM19239	blood:	n/a
29	chr1:58715539-58715589	A549	lung:	n/a
30	chr1:58715744-58715794	SAEC	small airway:	n/a
31	chr1:58717632-58717682	BE2_C	brain:	n/a
32	chr1:58718544-58718594	AoSMC	blood vessel:	n/a
33	chr1:58713941-58713991	GM12891	blood:	n/a
34	chr1:58717632-58717682	SAEC	small airway:	n/a
35	chr1:58716377-58716427	GM12891	blood:	n/a
36	chr1:58715553-58715603	NT2-D1	testis:	n/a
37	chr1:58714305-58714355	NH-A	brain:	n/a
38	chr1:58716306-58716356	T-47D	breast:	n/a
39	chr1:58715539-58715589	Hela-S3	cervix:	n/a
40	chr1:58714305-58714355	ProgFib	skin:	n/a
41	chr1:58716033-58716083	CMK	blood:	n/a
42	chr1:58715499-58715549	HL-60	blood:	n/a
43	chr1:58716018-58716068	PFSK-1	brain:	n/a
44	chr1:58716018-58716068	ovcar-3	ovarian:	n/a
45	chr1:58715553-58715603	SK-N-SH	brain:	n/a
46	chr1:58715747-58715797	U87	brain:	n/a
47	chr1:58717632-58717682	GM06990	blood:	n/a
48	chr1:58716033-58716083	HEEpiC	esophagus:	n/a
49	chr1:58712062-58712112	HNPCEpiC	eye:	n/a
50	chr1:58715539-58715589	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:58722434..58724317-chr1:58724409..58727876,3	K562	blood:
2	chr1:58711426..58714604-chr1:58717021..58720890,3	K562	blood:
3	chr1:58711426..58714604-chr1:58717021..58720890,3	K562	blood:
4	chr1:58722434..58724317-chr1:58724409..58727876,3	K562	blood:
5	chr1:58710082..58711946-chr1:58713535..58716517,2	K562	blood:
6	chr1:58722416..58724317-chr1:58724409..58727199,2	K562	blood:
7	chr1:58717073..58717741-chr1:59012205..59012834,2	K562	blood:
8	chr1:58722416..58724317-chr1:58724409..58727199,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OMA1-2	chr1:58706187-58707265	ucscGeneNc_uc001cyw_1

No data

Variant related genes	Relation type
DAB1	TF binding region
DAB1	CpG island
ENSG00000173406	chromatin interactions
ENSG00000162600	chromatin interactions

Extended variants
information (count: 898 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:898 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs494214	chr1:58707111-58707112	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565189043	chr1:58707167-58707168	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs495179	chr1:58707234-58707235	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs112247460	chr1:58707239-58707240	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs542566719	chr1:58707251-58707252	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs35943840	chr1:58707257-58707258	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs112925651	chr1:58707293-58707294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78602249	chr1:58707311-58707312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs7556433	chr1:58707353-58707354	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs547054199	chr1:58707519-58707520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186859125	chr1:58707654-58707655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538808913	chr1:58707708-58707709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558894046	chr1:58707772-58707773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575569529	chr1:58707780-58707781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113472716	chr1:58707902-58707903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs148099402	chr1:58707929-58707930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190053119	chr1:58707946-58707947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12034905	chr1:58707947-58707948	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs143836441	chr1:58707973-58707974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs559784751	chr1:58707977-58707978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs147260974	chr1:58708019-58708020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111769522	chr1:58708066-58708067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182323323	chr1:58708069-58708070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552987311	chr1:58708075-58708076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551233353	chr1:58708077-58708078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561159187	chr1:58708119-58708120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs75161694	chr1:58708152-58708153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547138240	chr1:58708171-58708172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566924038	chr1:58708258-58708259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs115229941	chr1:58708315-58708316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs115906838	chr1:58708368-58708369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569071907	chr1:58708447-58708448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564605580	chr1:58708468-58708469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537781236	chr1:58708488-58708489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554834761	chr1:58708520-58708521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs140832567	chr1:58708543-58708544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186532929	chr1:58708552-58708553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs71580860	chr1:58708573-58708574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533756419	chr1:58708637-58708638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553456569	chr1:58708646-58708647	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528445368	chr1:58708657-58708658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573027632	chr1:58708681-58708682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs142791188	chr1:58708744-58708745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs74077943	chr1:58708790-58708791	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371861220	chr1:58708828-58708829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558752447	chr1:58708894-58708895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200196870	chr1:58708913-58708914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575777307	chr1:58708941-58708942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542516262	chr1:58708972-58708973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544592742	chr1:58708985-58708986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
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
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
Meckel-Gruber syndrome	21572526	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	16616336	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:392 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:58702200-58713000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:58705200-58713000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr1:58705400-58712400	Weak transcription	Fetal Brain Male	brain
4	chr1:58705800-58708600	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr1:58708600-58708800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr1:58709600-58710000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr1:58709800-58710000	Enhancers	Brain Cingulate Gyrus	brain
8	chr1:58710000-58713000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr1:58710800-58711600	Enhancers	Liver	Liver
10	chr1:58712000-58712400	Enhancers	Fetal Brain Female	brain
11	chr1:58712400-58712800	Bivalent Enhancer	Fetal Brain Female	brain
12	chr1:58712400-58712800	ZNF genes & repeats	Gastric	stomach
13	chr1:58712400-58713800	Enhancers	Fetal Brain Male	brain
14	chr1:58713000-58713200	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr1:58713000-58713200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr1:58713000-58713600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
17	chr1:58713000-58713600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
18	chr1:58713000-58713800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr1:58713000-58713800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr1:58713000-58713800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
21	chr1:58713000-58713800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
22	chr1:58713000-58714200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
23	chr1:58713000-58714200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
24	chr1:58713000-58716800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
25	chr1:58713200-58713400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
26	chr1:58713200-58713600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr1:58713200-58713800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr1:58713200-58714400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
29	chr1:58713200-58714600	Bivalent/Poised TSS	Fetal Brain Female	brain
30	chr1:58713400-58713800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
31	chr1:58713400-58714200	Weak transcription	Gastric	stomach
32	chr1:58713600-58713800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr1:58713600-58713800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
34	chr1:58713600-58713800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
35	chr1:58713600-58713800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr1:58713600-58713800	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
37	chr1:58713600-58714000	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr1:58713600-58714000	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
39	chr1:58713600-58714200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
40	chr1:58713600-58714400	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr1:58713600-58714400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
42	chr1:58713600-58714600	Bivalent Enhancer	Liver	Liver
43	chr1:58713600-58715200	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
44	chr1:58713800-58714000	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr1:58713800-58714000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
46	chr1:58713800-58714000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
47	chr1:58713800-58714000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
48	chr1:58713800-58714000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr1:58713800-58714000	Bivalent Enhancer	Primary B cells from cord blood	blood
50	chr1:58713800-58714000	Bivalent Enhancer	Brain Anterior Caudate	brain

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