Variant report

Variant	esv1823889
Chromosome Location	chr2:76780130-76874809
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:442)
CpG islands
(count:122)
Chromatin interactive
region (count:6)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:442 , 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	ARID3A	chr2:76826892-76827267	HepG2	liver:	n/a	n/a
2	ATF2	chr2:76868112-76868533	GM12878	blood:	n/a	n/a
3	BACH1	chr2:76826863-76827150	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr2:76868153-76868459	GM12878	blood:	n/a	chr2:76868323-76868334 chr2:76868324-76868334 chr2:76868320-76868330
5	BATF	chr2:76826886-76827145	GM12878	blood:	n/a	n/a
6	BCL11A	chr2:76868123-76868435	GM12878	blood:	n/a	chr2:76868323-76868332 chr2:76868322-76868331
7	BHLHE40	chr2:76826935-76827215	GM12878	blood:	n/a	n/a
8	BHLHE40	chr2:76826921-76827181	K562	blood:	n/a	n/a
9	BRCA1	chr2:76826858-76827249	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr2:76796996-76797228	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr2:76797051-76797266	A549	lung:	n/a	n/a
12	CEBPB	chr2:76826891-76827167	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr2:76797647-76797927	A549	lung:	n/a	chr2:76797773-76797790 chr2:76797774-76797787 chr2:76797774-76797785 chr2:76797775-76797786
14	CEBPB	chr2:76797598-76797957	HepG2	liver:	n/a	chr2:76797773-76797790 chr2:76797774-76797787 chr2:76797774-76797785 chr2:76797775-76797786
15	CEBPB	chr2:76797009-76797286	IMR90	lung:	n/a	n/a
16	CEBPB	chr2:76797619-76797897	K562	blood:	n/a	chr2:76797773-76797790 chr2:76797774-76797787 chr2:76797774-76797785 chr2:76797775-76797786
17	CEBPB	chr2:76797632-76797940	IMR90	lung:	n/a	chr2:76797773-76797790 chr2:76797774-76797787 chr2:76797774-76797785 chr2:76797775-76797786
18	CEBPB	chr2:76797064-76797289	MCF-7	breast:	n/a	n/a
19	CEBPB	chr2:76796956-76797326	HepG2	liver:	n/a	n/a
20	CHD1	chr2:76808522-76808533	GM12878	blood:	n/a	n/a
21	CHD2	chr2:76826886-76827202	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr2:76791146-76791215	HepG2	liver:	n/a	n/a
23	CREB1	chr2:76856448-76856731	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr2:76826873-76827211	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr2:76826980-76827130	AG04449	skin:	n/a	n/a
26	CTCF	chr2:76826980-76827130	AG10803	skin:	n/a	n/a
27	CTCF	chr2:76826860-76827010	HFF-Myc	foreskin:	n/a	n/a
28	CTCF	chr2:76827040-76827190	AG09319	gingival:	n/a	n/a
29	CTCF	chr2:76826904-76827218	K562	blood:	n/a	n/a
30	CTCF	chr2:76826980-76827130	BJ	skin:	n/a	n/a
31	CTCF	chr2:76826940-76827090	MCF-7	breast:	n/a	n/a
32	CTCF	chr2:76826980-76827130	GM12870	blood:	n/a	n/a
33	CTCF	chr2:76827340-76827490	GM12870	blood:	n/a	n/a
34	CTCF	chr2:76827000-76827150	GM12872	blood:	n/a	n/a
35	CTCF	chr2:76826940-76827090	HCFaa	heart:	n/a	n/a
36	CTCF	chr2:76826818-76827279	HepG2	liver:	n/a	n/a
37	CTCF	chr2:76827000-76827150	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr2:76826891-76827222	GM13977	blood:	n/a	n/a
39	CTCF	chr2:76826910-76827146	MCF-7	breast:	n/a	n/a
40	CTCF	chr2:76826920-76827070	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:76826930-76827146	GM12892	blood:	n/a	n/a
42	CTCF	chr2:76826740-76826890	AG10803	skin:	n/a	n/a
43	CTCF	chr2:76826920-76827070	BE2_C	brain:	n/a	n/a
44	CTCF	chr2:76827000-76827150	AG09319	gingival:	n/a	n/a
45	CTCF	chr2:76827780-76827930	K562	blood:	n/a	n/a
46	CTCF	chr2:76826960-76827110	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr2:76826960-76827110	Caco-2	colon:	n/a	n/a
48	CTCF	chr2:76826980-76827130	Caco-2	colon:	n/a	n/a
49	CTCF	chr2:76826940-76827090	HAc	cerebellar:	n/a	n/a
50	CTCF	chr2:76868122-76868150	GM13976	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:76839078-76839128	Jurkat	blood:	n/a
2	chr2:76806361-76806411	PFSK-1	brain:	n/a
3	chr2:76839078-76839128	NT2-D1	testis:	n/a
4	chr2:76839078-76839128	RPTEC	kidney:	n/a
5	chr2:76839078-76839128	Hela-S3	cervix:	n/a
6	chr2:76839078-76839128	PANC-1	pancreas:	n/a
7	chr2:76839078-76839128	HCPEpiC	choroid plexus:	n/a
8	chr2:76839078-76839128	Hepatocyte	liver:	n/a
9	chr2:76839078-76839128	HAEpiC	amniotic membrane:	n/a
10	chr2:76806361-76806411	IMR90	lung:	fetal
11	chr2:76839078-76839128	ECC-1	luminal epithelium:	n/a
12	chr2:76839078-76839128	HCF	heart:	n/a
13	chr2:76839078-76839128	NHDF-neo	bronchial:	n/a
14	chr2:76806361-76806411	MCF10A-Er-Src	breast:	n/a
15	chr2:76839078-76839128	HepG2	liver:	n/a
16	chr2:76806361-76806411	AoSMC	blood vessel:	n/a
17	chr2:76806361-76806411	GM12878	blood:	n/a
18	chr2:76806361-76806411	SK-N-MC	brain:	n/a
19	chr2:76806361-76806411	T-47D	breast:	n/a
20	chr2:76806361-76806411	A549	lung:	n/a
21	chr2:76839078-76839128	BE2_C	brain:	n/a
22	chr2:76839078-76839128	HRE	kidney:	n/a
23	chr2:76839078-76839128	PFSK-1	brain:	n/a
24	chr2:76806361-76806411	AG10803	skin:	n/a
25	chr2:76806361-76806411	H1-hESC	embryonic stem cell:	embryo
26	chr2:76839078-76839128	AG04449	skin:	fetal
27	chr2:76839078-76839128	HNPCEpiC	eye:	n/a
28	chr2:76839078-76839128	NHBE	bronchial:	n/a
29	chr2:76839078-76839128	NB4	blood:	n/a
30	chr2:76839078-76839128	PrEC	prostate:	n/a
31	chr2:76839078-76839128	AoSMC	blood vessel:	n/a
32	chr2:76839078-76839128	MCF10A-Er-Src	breast:	n/a
33	chr2:76839078-76839128	HPAEpiC	pulmonary alveolar:	n/a
34	chr2:76806361-76806411	ECC-1	luminal epithelium:	n/a
35	chr2:76806361-76806411	SK-N-SH_RA	brain:	n/a
36	chr2:76839078-76839128	CMK	blood:	n/a
37	chr2:76839078-76839128	AG04450	lung:	fetal
38	chr2:76806361-76806411	HEEpiC	esophagus:	n/a
39	chr2:76806361-76806411	HepG2	liver:	n/a
40	chr2:76806361-76806411	NH-A	brain:	n/a
41	chr2:76839078-76839128	MCF-7	breast:	n/a
42	chr2:76839078-76839128	SKMC	muscle:	n/a
43	chr2:76806361-76806411	SAEC	small airway:	n/a
44	chr2:76806361-76806411	HPAEpiC	pulmonary alveolar:	n/a
45	chr2:76839078-76839128	T-47D	breast:	n/a
46	chr2:76806361-76806411	AG09309	skin:	n/a
47	chr2:76806361-76806411	Hepatocyte	liver:	n/a
48	chr2:76806361-76806411	Jurkat	blood:	n/a
49	chr2:76806361-76806411	CMK	blood:	n/a
50	chr2:76839078-76839128	HRPEpiC	eye:	n/a

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

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

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

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

No data

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

Extended variants
information (count: 4236 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:4236 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13400466	chr2:76780130-76780131	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs367571551	chr2:76780137-76780138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs1519994	chr2:76780139-76780140	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs568139028	chr2:76780150-76780151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs77384582	chr2:76780206-76780207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs75266933	chr2:76780217-76780218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs151249561	chr2:76780256-76780257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs569114149	chr2:76780288-76780289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs1519993	chr2:76780313-76780314	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs551898995	chr2:76780327-76780328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571062075	chr2:76780330-76780331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533960092	chr2:76780340-76780341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549164256	chr2:76780352-76780353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs377258695	chr2:76780365-76780366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs565693211	chr2:76780370-76780371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200844594	chr2:76780437-76780438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs201902672	chr2:76780441-76780442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs66532411	chr2:76780442-76780443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs57304438	chr2:76780444-76780445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs79830221	chr2:76780445-76780446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567573044	chr2:76780467-76780468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs367963336	chr2:76780542-76780543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7577486	chr2:76780558-76780559	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs558017664	chr2:76780578-76780579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs58787661	chr2:76780581-76780582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556134733	chr2:76780602-76780603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371352867	chr2:76780642-76780643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs140465667	chr2:76780650-76780651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538394120	chr2:76780685-76780686	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs80304429	chr2:76780691-76780692	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573137797	chr2:76780710-76780711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540444021	chr2:76780724-76780725	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs72810865	chr2:76780730-76780731	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs184525913	chr2:76780751-76780752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7604342	chr2:76780752-76780753	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs13387708	chr2:76780753-76780754	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs533340016	chr2:76780759-76780760	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554012935	chr2:76780778-76780779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189086778	chr2:76780826-76780827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181800137	chr2:76780942-76780943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368239308	chr2:76780965-76780966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74988296	chr2:76781022-76781023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs75120843	chr2:76781068-76781069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184985351	chr2:76781070-76781071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371083602	chr2:76781081-76781082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538180205	chr2:76781130-76781131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549805126	chr2:76781149-76781150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571252316	chr2:76781168-76781169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs111295311	chr2:76781171-76781172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs146643311	chr2:76781183-76781184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:295 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:76776000-76807000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:76778000-76780600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr2:76780600-76781000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr2:76783000-76783600	Enhancers	Liver	Liver
5	chr2:76788800-76789400	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr2:76789400-76793800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr2:76790800-76793000	Enhancers	Liver	Liver
8	chr2:76792000-76792400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr2:76792000-76792400	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr2:76792000-76792400	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr2:76793000-76796600	Weak transcription	Liver	Liver
12	chr2:76793400-76793800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr2:76793800-76794200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr2:76793800-76795200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
15	chr2:76793800-76798800	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr2:76794200-76794800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
17	chr2:76794800-76795400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
18	chr2:76795000-76797200	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr2:76795200-76797000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr2:76795400-76796800	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr2:76796600-76796800	Enhancers	Liver	Liver
22	chr2:76796800-76797200	Active TSS	Pancreatic Islets	Pancreatic Islet
23	chr2:76796800-76797600	Flanking Active TSS	Liver	Liver
24	chr2:76796800-76797800	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr2:76796800-76800000	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr2:76796800-76800600	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr2:76797000-76797600	Enhancers	Pancreas	Pancrea
28	chr2:76797000-76797800	Enhancers	Fetal Heart	heart
29	chr2:76797000-76800800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr2:76797200-76797600	Enhancers	H9 Cell Line	embryonic stem cell
31	chr2:76797200-76797600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr2:76797400-76797600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr2:76797600-76798600	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr2:76797600-76798800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr2:76797600-76800000	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr2:76797800-76798200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr2:76798200-76799000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr2:76798200-76799400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr2:76798200-76800000	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr2:76798600-76799200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr2:76798600-76799200	Enhancers	H9 Cell Line	embryonic stem cell
42	chr2:76798600-76799800	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr2:76798800-76799000	Enhancers	H1 Cell Line	embryonic stem cell
44	chr2:76798800-76800000	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr2:76798800-76800600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr2:76799000-76799800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
47	chr2:76799000-76799800	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr2:76799200-76799600	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr2:76799200-76800000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr2:76799600-76800200	Enhancers	H9 Cell Line	embryonic stem cell

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