Variant report

Variant	nsv832080
Chromosome Location	chr11:18882048-18975514
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:217)
CpG islands
(count:367)
Chromatin interactive
region (count:4)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:217 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr11:18887554-18887781	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr11:18946494-18946596	HepG2	liver:	n/a	chr11:18946576-18946587
3	CEBPB	chr11:18883944-18884278	Hela-S3	cervix:	n/a	chr11:18884110-18884121
4	CEBPB	chr11:18886183-18886383	IMR90	lung:	n/a	chr11:18886280-18886291
5	CEBPB	chr11:18886146-18886431	A549	lung:	n/a	chr11:18886280-18886291
6	CEBPB	chr11:18886185-18886385	HepG2	liver:	n/a	chr11:18886280-18886291
7	CEBPB	chr11:18965116-18965409	K562	blood:	n/a	n/a
8	CEBPB	chr11:18883959-18884233	IMR90	lung:	n/a	chr11:18884110-18884121
9	CEBPB	chr11:18943007-18943263	K562	blood:	n/a	n/a
10	CEBPB	chr11:18883950-18884225	A549	lung:	n/a	chr11:18884110-18884121
11	CEBPB	chr11:18970388-18970535	A549	lung:	n/a	n/a
12	CEBPB	chr11:18886294-18886322	K562	blood:	n/a	n/a
13	CEBPB	chr11:18883958-18884215	HepG2	liver:	n/a	chr11:18884110-18884121
14	CEBPB	chr11:18885553-18885558	A549	lung:	n/a	n/a
15	CEBPD	chr11:18965149-18965591	K562	blood:	n/a	n/a
16	CEBPD	chr11:18942867-18943456	K562	blood:	n/a	n/a
17	CTCF	chr11:18912305-18912431	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr11:18949160-18949310	HMEC	breast:	n/a	n/a
19	CTCF	chr11:18912314-18912425	NHEK	skin:	n/a	n/a
20	CTCF	chr11:18912280-18912430	RPTEC	kidney:	n/a	n/a
21	CTCF	chr11:18944088-18944127	GM20000	blood:	n/a	n/a
22	CTCF	chr11:18912302-18912431	MCF-7	breast:	n/a	n/a
23	CTCF	chr11:18912140-18912290	HCT-116	colon:	n/a	n/a
24	CTCF	chr11:18949160-18949310	NHEK	skin:	n/a	n/a
25	CTCF	chr11:18949060-18949210	RPTEC	kidney:	n/a	n/a
26	CTCF	chr11:18912200-18912350	NHEK	skin:	n/a	n/a
27	CTCF	chr11:18912319-18912427	MCF-7	breast:	n/a	n/a
28	CTCF	chr11:18944630-18944650	GM20000	blood:	n/a	n/a
29	CTCF	chr11:18912387-18912391	GM19239	blood:	n/a	n/a
30	CTCF	chr11:18951819-18951855	Fibrobl	skin:	n/a	n/a
31	CTCF	chr11:18949082-18949341	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr11:18912260-18912410	MCF-7	breast:	n/a	n/a
33	CTCF	chr11:18973940-18974063	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr11:18915764-18915770	GM10248	blood:	n/a	n/a
35	CTCF	chr11:18952280-18952430	HMF	breast:	n/a	n/a
36	CTCF	chr11:18912179-18912483	MCF-7	breast:	n/a	n/a
37	CTCF	chr11:18912260-18912410	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr11:18912280-18912430	A549	lung:	n/a	n/a
39	CTCF	chr11:18949100-18949250	RPTEC	kidney:	n/a	n/a
40	CTCF	chr11:18912320-18912470	MCF-7	breast:	n/a	n/a
41	CTCF	chr11:18912345-18912389	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr11:18912287-18912437	MCF-7	breast:	n/a	n/a
43	CTCF	chr11:18912340-18912490	HEK293	kidney:	n/a	n/a
44	CTCF	chr11:18949060-18949210	NHEK	skin:	n/a	n/a
45	CTCF	chr11:18949220-18949370	HMEC	breast:	n/a	n/a
46	CTCF	chr11:18949200-18949350	HEEpiC	esophagus:	n/a	n/a
47	CTCF	chr11:18912260-18912410	Caco-2	colon:	n/a	n/a
48	CTCF	chr11:18912280-18912430	HepG2	liver:	n/a	n/a
49	CTCF	chr11:18949130-18949280	K562	blood:	n/a	n/a
50	CTCF	chr11:18912320-18912470	Caco-2	colon:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:18957755-18957805	Hepatocyte	liver:	n/a
2	chr11:18957755-18957805	Hepatocyte	liver:	n/a
3	chr11:18955977-18956027	GM19239	blood:	n/a
4	chr11:18956196-18956246	GM06990	blood:	n/a
5	chr11:18956283-18956333	A549	lung:	n/a
6	chr11:18957755-18957805	ProgFib	skin:	n/a
7	chr11:18957755-18957805	NT2-D1	testis:	n/a
8	chr11:18955977-18956027	HepG2	liver:	n/a
9	chr11:18955977-18956027	T-47D	breast:	n/a
10	chr11:18956637-18956687	AG09319	gingival:	n/a
11	chr11:18955977-18956027	HL-60	blood:	n/a
12	chr11:18956283-18956333	Jurkat	blood:	n/a
13	chr11:18956637-18956687	RPTEC	kidney:	n/a
14	chr11:18887821-18887871	T-47D	breast:	n/a
15	chr11:18956196-18956246	MCF10A-Er-Src	breast:	n/a
16	chr11:18956637-18956687	SK-N-SH	brain:	n/a
17	chr11:18956196-18956246	BJ	skin:	n/a
18	chr11:18956196-18956246	PFSK-1	brain:	n/a
19	chr11:18887821-18887871	HPAEpiC	pulmonary alveolar:	n/a
20	chr11:18887821-18887871	U87	brain:	n/a
21	chr11:18956196-18956246	HMEC	breast:	n/a
22	chr11:18956196-18956246	IMR90	lung:	fetal
23	chr11:18956283-18956333	HepG2	liver:	n/a
24	chr11:18956283-18956333	HCM	heart:	n/a
25	chr11:18956283-18956333	HEK293	kidney:	embryo
26	chr11:18956283-18956333	MCF-7	breast:	n/a
27	chr11:18956283-18956333	T-47D	breast:	n/a
28	chr11:18956196-18956246	PrEC	prostate:	n/a
29	chr11:18956637-18956687	GM19239	blood:	n/a
30	chr11:18957755-18957805	PANC-1	pancreas:	n/a
31	chr11:18955977-18956027	SAEC	small airway:	n/a
32	chr11:18955977-18956027	IMR90	lung:	fetal
33	chr11:18956283-18956333	GM12891	blood:	n/a
34	chr11:18956283-18956333	Hepatocyte	liver:	n/a
35	chr11:18956283-18956333	GM06990	blood:	n/a
36	chr11:18956196-18956246	HL-60	blood:	n/a
37	chr11:18956637-18956687	PFSK-1	brain:	n/a
38	chr11:18887821-18887871	HCPEpiC	choroid plexus:	n/a
39	chr11:18956637-18956687	NH-A	brain:	n/a
40	chr11:18956196-18956246	Jurkat	blood:	n/a
41	chr11:18887821-18887871	NH-A	brain:	n/a
42	chr11:18956283-18956333	AoSMC	blood vessel:	n/a
43	chr11:18955977-18956027	Jurkat	blood:	n/a
44	chr11:18956637-18956687	HMEC	breast:	n/a
45	chr11:18957755-18957805	RPTEC	kidney:	n/a
46	chr11:18955977-18956027	HCM	heart:	n/a
47	chr11:18957755-18957805	NB4	blood:	n/a
48	chr11:18957755-18957805	SAEC	small airway:	n/a
49	chr11:18955977-18956027	AG09319	gingival:	n/a
50	chr11:18957755-18957805	AG10803	skin:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:18898429..18900473-chr11:18904147..18906021,2	K562	blood:
2	chr11:18948757..18949726-chr11:19092570..19093333,3	MCF-7	breast:
3	chr11:18898429..18900473-chr11:18904147..18906021,2	K562	blood:
4	chr11:18951880..18953861-chr11:18956190..18958282,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZDHHC13-2	chr11:18956532-18956821	ENSG00000255244.1
2	lnc-ZDHHC13-2	chr11:18960852-18961268	ENSG00000255244.1
3	lnc-MRGPRX1-1	chr11:18885105-18886056	NONHSAT018323

No data

Variant related genes	Relation type
ENSG00000255536	TF binding region
ENSG00000254541	TF binding region
MRGPRX1	TF binding region
ENSG00000255244	TF binding region
ENSG00000255511	TF binding region
ENSG00000254529	TF binding region
ENSG00000255536	CpG island
ENSG00000254541	CpG island
MRGPRX1	CpG island
ENSG00000255244	CpG island
ENSG00000255511	CpG island
ENSG00000254529	CpG island
ENSG00000170255	chromatin interactions
ENSG00000255244	chromatin interactions

Extended variants
information (count: 2087 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2087 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138901891	chr11:18882081-18882082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs117060716	chr11:18882122-18882123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs540529800	chr11:18882173-18882174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149396881	chr11:18882215-18882216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs6483543	chr11:18882221-18882222	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs147167764	chr11:18882237-18882238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113564409	chr11:18882261-18882262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536698993	chr11:18882308-18882309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371001592	chr11:18882354-18882355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576946411	chr11:18882356-18882357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566607472	chr11:18882393-18882394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs527239500	chr11:18882436-18882437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552159832	chr11:18882446-18882447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571820313	chr11:18882487-18882488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4303219	chr11:18882536-18882537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs80356170	chr11:18882549-18882550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569100342	chr11:18882585-18882586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76397706	chr11:18882603-18882604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544422107	chr11:18882612-18882613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562808344	chr11:18882691-18882692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192281290	chr11:18882701-18882702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs573299437	chr11:18882703-18882704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs75004281	chr11:18882707-18882708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182990941	chr11:18882774-18882775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs577335104	chr11:18882777-18882778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544499792	chr11:18882848-18882849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562809347	chr11:18882893-18882894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530145353	chr11:18882915-18882916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574679485	chr11:18882946-18882947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541775447	chr11:18882989-18882990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370576738	chr11:18883044-18883045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs10766512	chr11:18883099-18883100	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs527396470	chr11:18883112-18883113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552014064	chr11:18883123-18883124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563723836	chr11:18883137-18883138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531247358	chr11:18883182-18883183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs115623868	chr11:18883183-18883184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs76777443	chr11:18883228-18883229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs61886504	chr11:18883270-18883271	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs115190951	chr11:18883296-18883297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566821179	chr11:18883306-18883307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534274210	chr11:18883309-18883310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558815495	chr11:18883336-18883337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577299930	chr11:18883341-18883342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538287521	chr11:18883391-18883392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556448954	chr11:18883399-18883400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550363729	chr11:18883409-18883410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187897363	chr11:18883444-18883445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541626173	chr11:18883445-18883446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560273526	chr11:18883458-18883459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Ollier disease	21235737	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:18881800-18899800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:18884200-18884800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr11:18886200-18886600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr11:18886400-18887200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr11:18886400-18888600	Enhancers	H1 Cell Line	embryonic stem cell
6	chr11:18886600-18887000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr11:18886600-18887200	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr11:18886600-18887200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr11:18886600-18888600	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr11:18886800-18887200	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr11:18886800-18887400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr11:18886800-18887800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr11:18886800-18888200	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr11:18886800-18888600	Enhancers	H9 Cell Line	embryonic stem cell
15	chr11:18887000-18887400	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr11:18887000-18887600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
17	chr11:18887000-18888600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr11:18887200-18887600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr11:18887200-18887600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
20	chr11:18887200-18887600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
21	chr11:18887200-18887600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr11:18887400-18887600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr11:18887600-18887800	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr11:18887600-18887800	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr11:18887600-18887800	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr11:18887600-18887800	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr11:18887600-18888000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr11:18887600-18888400	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr11:18887800-18888000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
30	chr11:18887800-18888000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
31	chr11:18887800-18888000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
32	chr11:18887800-18888600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
33	chr11:18888000-18888400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr11:18888000-18888400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr11:18888000-18888400	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr11:18888000-18888400	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr11:18890200-18890400	Bivalent/Poised TSS	Muscle Satellite Cultured Cells	--
38	chr11:18897400-18897600	Flanking Bivalent TSS/Enh	Left Ventricle	heart
39	chr11:18899600-18900200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr11:18907600-18908000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
41	chr11:18908000-18908600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr11:18915200-18922000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr11:18918200-18919600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr11:18918400-18918600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr11:18919000-18919200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr11:18919200-18919600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr11:18919600-18920400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr11:18919600-18921400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr11:18920400-18921000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr11:18920800-18923000	Enhancers	HepG2	liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links