Variant report

Variant	esv1820363
Chromosome Location	chr2:76812833-76859952
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:313)
CpG islands
(count:62)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:313 , 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	CHD2	chr2:76826886-76827202	H1-hESC	embryonic stem cell:	n/a	n/a
9	CREB1	chr2:76856448-76856731	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr2:76822187-76822219	GM20000	blood:	n/a	n/a
11	CTCF	chr2:76826960-76827110	GM12865	blood:	n/a	n/a
12	CTCF	chr2:76826640-76826790	GM12865	blood:	n/a	n/a
13	CTCF	chr2:76826927-76827189	GM20000	blood:	n/a	n/a
14	CTCF	chr2:76826980-76827130	GM12871	blood:	n/a	n/a
15	CTCF	chr2:76826920-76827070	HFF	foreskin:	n/a	n/a
16	CTCF	chr2:76826962-76827174	Lung_OC	lung:	n/a	n/a
17	CTCF	chr2:76826980-76827130	Caco-2	colon:	n/a	n/a
18	CTCF	chr2:76826960-76827110	GM12801	blood:	n/a	n/a
19	CTCF	chr2:76826869-76827175	HepG2	liver:	n/a	n/a
20	CTCF	chr2:76826760-76826910	AoAF	blood vessel:	n/a	n/a
21	CTCF	chr2:76826980-76827130	HL-60	blood:	n/a	n/a
22	CTCF	chr2:76827020-76827170	AG09309	skin:	n/a	n/a
23	CTCF	chr2:76826980-76827130	GM12875	blood:	n/a	n/a
24	CTCF	chr2:76826920-76827070	BE2_C	brain:	n/a	n/a
25	CTCF	chr2:76826980-76827130	HRPEpiC	eye:	n/a	n/a
26	CTCF	chr2:76826907-76827230	Pancreas_OC	pancreas:	n/a	n/a
27	CTCF	chr2:76827000-76827150	HepG2	liver:	n/a	n/a
28	CTCF	chr2:76826804-76827231	K562	blood:	n/a	n/a
29	CTCF	chr2:76826904-76827218	K562	blood:	n/a	n/a
30	CTCF	chr2:76827382-76827436	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr2:76827320-76827470	GM12864	blood:	n/a	n/a
32	CTCF	chr2:76851649-76851739	LNCaP	prostate:	n/a	n/a
33	CTCF	chr2:76826917-76827207	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr2:76826960-76827110	NHEK	skin:	n/a	n/a
35	CTCF	chr2:76826980-76827130	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr2:76827000-76827150	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr2:76826980-76827130	GM12867	blood:	n/a	n/a
38	CTCF	chr2:76826960-76827110	GM12874	blood:	n/a	n/a
39	CTCF	chr2:76826980-76827130	GM12868	blood:	n/a	n/a
40	CTCF	chr2:76826940-76827090	GM12867	blood:	n/a	n/a
41	CTCF	chr2:76826960-76827110	SAEC	small airway:	n/a	n/a
42	CTCF	chr2:76826920-76827070	MCF-7	breast:	n/a	n/a
43	CTCF	chr2:76826877-76827237	GM12878	blood:	n/a	n/a
44	CTCF	chr2:76826702-76827499	SK-N-SH	brain:	n/a	n/a
45	CTCF	chr2:76827000-76827150	AG10803	skin:	n/a	n/a
46	CTCF	chr2:76826960-76827110	HRE	kidney:	n/a	n/a
47	CTCF	chr2:76827000-76827150	NHLF	lung:	n/a	n/a
48	CTCF	chr2:76826960-76827110	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr2:76826960-76827110	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr2:76826740-76826890	AG10803	skin:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:76839078-76839128	NH-A	brain:	n/a
2	chr2:76839078-76839128	NH-A	brain:	n/a
3	chr2:76839078-76839128	Caco-2	colon:	n/a
4	chr2:76839078-76839128	GM06990	blood:	n/a
5	chr2:76839078-76839128	PFSK-1	brain:	n/a
6	chr2:76839078-76839128	GM19239	blood:	n/a
7	chr2:76839078-76839128	GM12878	blood:	n/a
8	chr2:76839078-76839128	GM12891	blood:	n/a
9	chr2:76839078-76839128	CMK	blood:	n/a
10	chr2:76839078-76839128	AG09309	skin:	n/a
11	chr2:76839078-76839128	IMR90	lung:	fetal
12	chr2:76839078-76839128	HRE	kidney:	n/a
13	chr2:76839078-76839128	SK-N-SH_RA	brain:	n/a
14	chr2:76839078-76839128	HUVEC	blood vessel:	n/a
15	chr2:76839078-76839128	NB4	blood:	n/a
16	chr2:76839078-76839128	BE2_C	brain:	n/a
17	chr2:76839078-76839128	LNCaP	prostate:	n/a
18	chr2:76839078-76839128	A549	lung:	n/a
19	chr2:76839078-76839128	HCF	heart:	n/a
20	chr2:76839078-76839128	NHBE	bronchial:	n/a
21	chr2:76839078-76839128	HCPEpiC	choroid plexus:	n/a
22	chr2:76839078-76839128	GM12892	blood:	n/a
23	chr2:76839078-76839128	ovcar-3	ovarian:	n/a
24	chr2:76839078-76839128	U87	brain:	n/a
25	chr2:76839078-76839128	Jurkat	blood:	n/a
26	chr2:76839078-76839128	RPTEC	kidney:	n/a
27	chr2:76839078-76839128	SKMC	muscle:	n/a
28	chr2:76839078-76839128	SK-N-SH	brain:	n/a
29	chr2:76839078-76839128	HNPCEpiC	eye:	n/a
30	chr2:76839078-76839128	ProgFib	skin:	n/a
31	chr2:76839078-76839128	MCF10A-Er-Src	breast:	n/a
32	chr2:76839078-76839128	HCM	heart:	n/a
33	chr2:76839078-76839128	HRPEpiC	eye:	n/a
34	chr2:76839078-76839128	AG04449	skin:	fetal
35	chr2:76839078-76839128	Hepatocyte	liver:	n/a
36	chr2:76839078-76839128	PANC-1	pancreas:	n/a
37	chr2:76839078-76839128	HEEpiC	esophagus:	n/a
38	chr2:76839078-76839128	AG10803	skin:	n/a
39	chr2:76839078-76839128	HCT-116	colon:	n/a
40	chr2:76839078-76839128	Hela-S3	cervix:	n/a
41	chr2:76839078-76839128	HPAEpiC	pulmonary alveolar:	n/a
42	chr2:76839078-76839128	HRCEpiC	kidney:	n/a
43	chr2:76839078-76839128	MCF-7	breast:	n/a
44	chr2:76839078-76839128	AG09319	gingival:	n/a
45	chr2:76839078-76839128	AoSMC	blood vessel:	n/a
46	chr2:76839078-76839128	SAEC	small airway:	n/a
47	chr2:76839078-76839128	K562	blood:	n/a
48	chr2:76839078-76839128	T-47D	breast:	n/a
49	chr2:76839078-76839128	HL-60	blood:	n/a
50	chr2:76839078-76839128	ECC-1	luminal epithelium:	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	chr2:76837968..76839669-chr2:76845469..76848246,2	MCF-7	breast:
4	chr2:76123697..76124563-chr2:76826531..76827162,2	MCF-7	breast:
5	chr2:76424788..76425711-chr2:76826568..76827565,9	MCF-7	breast:
6	chr2:76014514..76015446-chr2:76826422..76827585,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRPL19-18	chr2:76814741-76814827	NONHSAT071820
2	lnc-LRRTM4-5	chr2:76822539-76822804	NONHSAT071821

No data

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

Extended variants
information (count: 2111 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2111 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187401485	chr2:76812854-76812855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs548289838	chr2:76812881-76812882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192074777	chr2:76812882-76812883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs114935119	chr2:76812889-76812890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs199764044	chr2:76812896-76812897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs200317657	chr2:76812897-76812898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs397985055	chr2:76812921-76812922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201978204	chr2:76812922-76812923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs199908479	chr2:76812923-76812924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs201202215	chr2:76812924-76812925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540812223	chr2:76812931-76812932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs13002953	chr2:76812932-76812933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs13026694	chr2:76812940-76812941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs13026695	chr2:76812942-76812943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562393583	chr2:76812952-76812953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs13002968	chr2:76812961-76812962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529607780	chr2:76812968-76812969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs13026873	chr2:76812985-76812986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs13026875	chr2:76812992-76812993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551037806	chr2:76812994-76812995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs13026886	chr2:76813007-76813008	Genic enhancers Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs13026556	chr2:76813027-76813028	Genic enhancers Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs13003178	chr2:76813031-76813032	Genic enhancers Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs13003187	chr2:76813044-76813045	Genic enhancers Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569286619	chr2:76813045-76813046	Genic enhancers Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs142781646	chr2:76813062-76813063	Genic enhancers Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs184667465	chr2:76813083-76813084	Genic enhancers Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs566922996	chr2:76813098-76813099	Genic enhancers Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs146051822	chr2:76813147-76813148	Genic enhancers Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs13393400	chr2:76813163-76813164	Genic enhancers Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs376271602	chr2:76813174-76813175	Genic enhancers Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs11893233	chr2:76813189-76813190	Genic enhancers Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs537757374	chr2:76813226-76813227	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs373819216	chr2:76813243-76813244	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs201876792	chr2:76813246-76813247	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs75185008	chr2:76813254-76813255	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs11678705	chr2:76813255-76813256	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs371650731	chr2:76813269-76813270	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544954765	chr2:76813271-76813272	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs375056925	chr2:76813283-76813284	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs562556837	chr2:76813295-76813296	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs200366825	chr2:76813321-76813322	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs189434927	chr2:76813327-76813328	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs112906918	chr2:76813329-76813330	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs149840951	chr2:76813338-76813339	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs553847136	chr2:76813347-76813348	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs117646573	chr2:76813404-76813405	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs544925452	chr2:76813405-76813406	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563171509	chr2:76813417-76813418	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs533188608	chr2:76813429-76813430	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:76807400-76826800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:76808600-76824200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr2:76808800-76822200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr2:76810200-76813600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr2:76810400-76826200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr2:76811000-76813000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr2:76811200-76813000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr2:76811800-76816000	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr2:76813000-76813200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
10	chr2:76813000-76814200	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr2:76813000-76814200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr2:76813200-76814000	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr2:76813600-76816400	Strong transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr2:76814000-76817000	Strong transcription	HUES6 Cell Line	embryonic stem cell
15	chr2:76814200-76816600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr2:76814200-76826400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr2:76816000-76817000	Strong transcription	HUES48 Cell Line	embryonic stem cell
18	chr2:76816400-76817200	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
19	chr2:76816600-76817000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
20	chr2:76817000-76819200	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr2:76817000-76819400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr2:76817000-76826600	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr2:76817200-76849600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr2:76819200-76823200	Strong transcription	HUES6 Cell Line	embryonic stem cell
25	chr2:76819400-76819800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
26	chr2:76819800-76821000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr2:76821000-76823400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
28	chr2:76823200-76829400	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr2:76823400-76826800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr2:76824200-76824400	Enhancers	H9 Cell Line	embryonic stem cell
31	chr2:76824400-76825000	Enhancers	Gastric	stomach
32	chr2:76826200-76827000	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr2:76826400-76827400	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr2:76826600-76827400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr2:76826800-76827000	Enhancers	H9 Cell Line	embryonic stem cell
36	chr2:76826800-76827000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr2:76826800-76827400	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr2:76826800-76827600	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr2:76826800-76827600	Enhancers	Brain Hippocampus Middle	brain
40	chr2:76827400-76837600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr2:76827600-76828600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr2:76828600-76829000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr2:76829000-76837200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr2:76829200-76829800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr2:76829400-76829800	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr2:76835600-76835800	Enhancers	H1 Cell Line	embryonic stem cell
47	chr2:76835800-76837800	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr2:76836400-76836600	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr2:76836600-76837400	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr2:76836800-76842600	Enhancers	HUES48 Cell Line	embryonic stem cell

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