Variant report

Variant	esv1818817
Chromosome Location	chr2:76798873-76859557
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:333)
CpG islands
(count:123)
Chromatin interactive
region (count:6)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:333 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:76826892-76827267	HepG2	liver:	n/a	n/a
2	BACH1	chr2:76826863-76827150	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr2:76826886-76827145	GM12878	blood:	n/a	n/a
4	BHLHE40	chr2:76826921-76827181	K562	blood:	n/a	n/a
5	BHLHE40	chr2:76826935-76827215	GM12878	blood:	n/a	n/a
6	BRCA1	chr2:76826858-76827249	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr2:76826891-76827167	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD1	chr2:76808522-76808533	GM12878	blood:	n/a	n/a
9	CHD2	chr2:76826886-76827202	H1-hESC	embryonic stem cell:	n/a	n/a
10	CREB1	chr2:76856448-76856731	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr2:76826940-76827090	GM12874	blood:	n/a	n/a
12	CTCF	chr2:76827382-76827436	HUVEC	blood vessel:	n/a	n/a
13	CTCF	chr2:76826960-76827110	WERI-Rb-1	eye:	n/a	n/a
14	CTCF	chr2:76826892-76827198	HepG2	liver:	n/a	n/a
15	CTCF	chr2:76827040-76827190	BE2_C	brain:	n/a	n/a
16	CTCF	chr2:76826822-76827337	HCT-116	colon:	n/a	n/a
17	CTCF	chr2:76826940-76827090	MCF-7	breast:	n/a	n/a
18	CTCF	chr2:76826888-76827197	LNCaP	prostate:	n/a	n/a
19	CTCF	chr2:76827280-76827430	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr2:76826917-76827237	HUVEC	blood vessel:	n/a	n/a
21	CTCF	chr2:76856360-76856510	HepG2	liver:	n/a	n/a
22	CTCF	chr2:76826960-76827110	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr2:76826622-76827481	A549	lung:	n/a	n/a
24	CTCF	chr2:76827000-76827150	BJ	skin:	n/a	n/a
25	CTCF	chr2:76826894-76827232	K562	blood:	n/a	n/a
26	CTCF	chr2:76826920-76827070	HCT-116	colon:	n/a	n/a
27	CTCF	chr2:76826960-76827110	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr2:76826980-76827130	HEK293	kidney:	n/a	n/a
29	CTCF	chr2:76822187-76822219	GM20000	blood:	n/a	n/a
30	CTCF	chr2:76826980-76827130	GM12867	blood:	n/a	n/a
31	CTCF	chr2:76826960-76827110	Caco-2	colon:	n/a	n/a
32	CTCF	chr2:76826920-76827070	RPTEC	kidney:	n/a	n/a
33	CTCF	chr2:76827060-76827210	HCT-116	colon:	n/a	n/a
34	CTCF	chr2:76826910-76827137	MCF-7	breast:	n/a	n/a
35	CTCF	chr2:76826900-76827050	HAc	cerebellar:	n/a	n/a
36	CTCF	chr2:76826724-76827436	GM12878	blood:	n/a	n/a
37	CTCF	chr2:76827358-76827442	Fibrobl	skin:	n/a	n/a
38	CTCF	chr2:76826980-76827130	GM12865	blood:	n/a	n/a
39	CTCF	chr2:76851646-76851678	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr2:76826913-76827207	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr2:76827000-76827150	AG10803	skin:	n/a	n/a
42	CTCF	chr2:76826980-76827130	GM12872	blood:	n/a	n/a
43	CTCF	chr2:76826925-76827140	NHEK	skin:	n/a	n/a
44	CTCF	chr2:76826934-76827210	GM10266	blood:	n/a	n/a
45	CTCF	chr2:76826810-76827289	K562	blood:	n/a	n/a
46	CTCF	chr2:76826964-76827247	A549	lung:	n/a	n/a
47	CTCF	chr2:76826909-76827127	MCF-7	breast:	n/a	n/a
48	CTCF	chr2:76826980-76827130	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr2:76827040-76827190	AG09319	gingival:	n/a	n/a
50	CTCF	chr2:76826640-76826790	GM12865	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:76806361-76806411	AG04450	lung:	fetal
2	chr2:76806361-76806411	AG04450	lung:	fetal
3	chr2:76839078-76839128	Hepatocyte	liver:	n/a
4	chr2:76806361-76806411	HRE	kidney:	n/a
5	chr2:76839078-76839128	BE2_C	brain:	n/a
6	chr2:76806361-76806411	BJ	skin:	n/a
7	chr2:76839078-76839128	HNPCEpiC	eye:	n/a
8	chr2:76839078-76839128	NHDF-neo	bronchial:	n/a
9	chr2:76806361-76806411	HRCEpiC	kidney:	n/a
10	chr2:76806361-76806411	NHBE	bronchial:	n/a
11	chr2:76839078-76839128	HAEpiC	amniotic membrane:	n/a
12	chr2:76806361-76806411	ECC-1	luminal epithelium:	n/a
13	chr2:76839078-76839128	AG10803	skin:	n/a
14	chr2:76839078-76839128	HRPEpiC	eye:	n/a
15	chr2:76806361-76806411	GM06990	blood:	n/a
16	chr2:76806361-76806411	ProgFib	skin:	n/a
17	chr2:76806361-76806411	NHDF-neo	bronchial:	n/a
18	chr2:76806361-76806411	MCF-7	breast:	n/a
19	chr2:76806361-76806411	HEEpiC	esophagus:	n/a
20	chr2:76839078-76839128	HL-60	blood:	n/a
21	chr2:76806361-76806411	HRPEpiC	eye:	n/a
22	chr2:76839078-76839128	HEK293	kidney:	embryo
23	chr2:76806361-76806411	A549	lung:	n/a
24	chr2:76839078-76839128	NT2-D1	testis:	n/a
25	chr2:76839078-76839128	NB4	blood:	n/a
26	chr2:76839078-76839128	HCPEpiC	choroid plexus:	n/a
27	chr2:76806361-76806411	SK-N-SH_RA	brain:	n/a
28	chr2:76839078-76839128	CMK	blood:	n/a
29	chr2:76806361-76806411	HCF	heart:	n/a
30	chr2:76839078-76839128	HIPEpiC	eye:	n/a
31	chr2:76806361-76806411	K562	blood:	n/a
32	chr2:76839078-76839128	K562	blood:	n/a
33	chr2:76806361-76806411	PFSK-1	brain:	n/a
34	chr2:76806361-76806411	SK-N-SH	brain:	n/a
35	chr2:76806361-76806411	AG04449	skin:	fetal
36	chr2:76839078-76839128	Caco-2	colon:	n/a
37	chr2:76839078-76839128	IMR90	lung:	fetal
38	chr2:76806361-76806411	RPTEC	kidney:	n/a
39	chr2:76839078-76839128	HPAEpiC	pulmonary alveolar:	n/a
40	chr2:76806361-76806411	AG09309	skin:	n/a
41	chr2:76806361-76806411	MCF10A-Er-Src	breast:	n/a
42	chr2:76839078-76839128	MCF10A-Er-Src	breast:	n/a
43	chr2:76806361-76806411	HUVEC	blood vessel:	n/a
44	chr2:76806361-76806411	HCPEpiC	choroid plexus:	n/a
45	chr2:76806361-76806411	ovcar-3	ovarian:	n/a
46	chr2:76806361-76806411	SK-N-MC	brain:	n/a
47	chr2:76806361-76806411	HL-60	blood:	n/a
48	chr2:76806361-76806411	Caco-2	colon:	n/a
49	chr2:76839078-76839128	GM12892	blood:	n/a
50	chr2:76839078-76839128	GM12891	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:75957100..75957649-chr2:76826627..76827405,2	MCF-7	breast:
2	chr2:76837968..76839669-chr2:76845469..76848246,2	MCF-7	breast:
3	chr2:76424788..76425711-chr2:76826568..76827565,9	MCF-7	breast:
4	chr2:76837968..76839669-chr2:76845469..76848246,2	MCF-7	breast:
5	chr2:76123697..76124563-chr2:76826531..76827162,2	MCF-7	breast:
6	chr2:76014514..76015446-chr2:76826422..76827585,4	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRPL19-18	chr2:76806776-76806856	NONHSAT071820
2	lnc-LRRTM4-5	chr2:76822539-76822804	NONHSAT071821
3	lnc-MRPL19-18	chr2:76802723-76802739	NONHSAT071820
4	lnc-MRPL19-18	chr2:76807165-76807212	NONHSAT071820
5	lnc-MRPL19-18	chr2:76814741-76814827	NONHSAT071820
6	lnc-MRPL19-17	chr2:76802439-76802582	NONHSAT071819
7	lnc-MRPL19-17	chr2:76805608-76805913	NONHSAT071819

No data

Variant related genes	Relation type
RN7SKP164	TF binding region
RN7SKP164	CpG island

Extended variants
information (count: 2866 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2866 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112362932	chr2:76798902-76798903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs150966483	chr2:76798903-76798904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566084987	chr2:76798918-76798919	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs111840302	chr2:76798963-76798964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369226993	chr2:76798985-76798986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533622927	chr2:76798993-76798994	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73938476	chr2:76799006-76799007	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs149672334	chr2:76799009-76799010	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541979670	chr2:76799029-76799030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562239918	chr2:76799036-76799037	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557374608	chr2:76799058-76799059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537695483	chr2:76799066-76799067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6727579	chr2:76799126-76799127	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs547631743	chr2:76799150-76799151	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564489765	chr2:76799220-76799221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112023409	chr2:76799221-76799222	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540726565	chr2:76799269-76799270	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559898061	chr2:76799310-76799311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561902095	chr2:76799322-76799323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369956728	chr2:76799330-76799331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140415330	chr2:76799331-76799332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550746058	chr2:76799348-76799349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569077197	chr2:76799372-76799373	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs527350761	chr2:76799379-76799380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533241773	chr2:76799397-76799398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs77941085	chr2:76799460-76799461	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112921245	chr2:76799473-76799474	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10193489	chr2:76799495-76799496	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs533684120	chr2:76799632-76799633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548677651	chr2:76799633-76799634	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141055253	chr2:76799695-76799696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs73938477	chr2:76799700-76799701	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs376642548	chr2:76799753-76799754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371236573	chr2:76799834-76799835	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs148118604	chr2:76799856-76799857	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs111761763	chr2:76799878-76799879	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs573265224	chr2:76799879-76799880	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs190566486	chr2:76799889-76799890	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs150195025	chr2:76799933-76799934	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs113178616	chr2:76799979-76799980	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs142994370	chr2:76800123-76800124	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs147546531	chr2:76800149-76800150	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533125126	chr2:76800165-76800166	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs28651854	chr2:76800193-76800194	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs560150929	chr2:76800199-76800200	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527294631	chr2:76800246-76800247	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548542249	chr2:76800277-76800278	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567038771	chr2:76800285-76800286	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537533575	chr2:76800313-76800314	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138529940	chr2:76800351-76800352	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Mental retardation	17124404	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17440070	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Breast cancer	16272173	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	20531469	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:240 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:76776000-76807000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:76796800-76800000	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr2:76796800-76800600	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr2:76797000-76800800	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr2:76797600-76800000	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr2:76798200-76799000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr2:76798200-76799400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr2:76798200-76800000	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr2:76798600-76799200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr2:76798600-76799200	Enhancers	H9 Cell Line	embryonic stem cell
11	chr2:76798600-76799800	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr2:76798800-76799000	Enhancers	H1 Cell Line	embryonic stem cell
13	chr2:76798800-76800000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr2:76798800-76800600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr2:76799000-76799800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr2:76799000-76799800	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr2:76799200-76799600	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr2:76799200-76800000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr2:76799600-76800200	Enhancers	H9 Cell Line	embryonic stem cell
20	chr2:76799800-76800200	Enhancers	H1 Cell Line	embryonic stem cell
21	chr2:76799800-76800200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr2:76799800-76800600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr2:76800000-76800200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr2:76800000-76800200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr2:76800000-76800200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
26	chr2:76800000-76800600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
27	chr2:76800000-76800800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
28	chr2:76800200-76800400	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr2:76800200-76800400	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr2:76800200-76800400	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr2:76800400-76800600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
32	chr2:76800400-76800600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
33	chr2:76800400-76800600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr2:76800600-76800800	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr2:76800600-76801200	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr2:76800600-76801600	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr2:76800600-76802000	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr2:76800600-76804200	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr2:76800800-76801000	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr2:76800800-76801200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr2:76800800-76801800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr2:76801000-76801400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr2:76801200-76801400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr2:76801200-76802000	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr2:76801400-76801600	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr2:76801400-76802000	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr2:76801600-76803200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr2:76801600-76805200	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr2:76801800-76802000	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr2:76802000-76802800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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