Variant report

Variant	nsv555097
Chromosome Location	chr11:56084611-56235061
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr11:56138124-56138366	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr11:56147615-56147939	Hela-S3	cervix:	n/a	chr11:56147786-56147799 chr11:56147786-56147797 chr11:56147786-56147799 chr11:56147788-56147797 chr11:56147788-56147797 chr11:56147788-56147797
3	CEBPB	chr11:56172033-56172106	H1-hESC	embryonic stem cell:	n/a	chr11:56172088-56172099
4	CEBPB	chr11:56147598-56147982	H1-hESC	embryonic stem cell:	n/a	chr11:56147786-56147799 chr11:56147786-56147797 chr11:56147786-56147799 chr11:56147788-56147797 chr11:56147788-56147797 chr11:56147788-56147797
5	CEBPB	chr11:56171929-56172241	A549	lung:	n/a	chr11:56172088-56172099
6	CEBPB	chr11:56147604-56147937	HepG2	liver:	n/a	chr11:56147786-56147799 chr11:56147786-56147797 chr11:56147786-56147799 chr11:56147788-56147797 chr11:56147788-56147797 chr11:56147788-56147797
7	CEBPB	chr11:56147618-56147932	A549	lung:	n/a	chr11:56147786-56147799 chr11:56147786-56147797 chr11:56147786-56147799 chr11:56147788-56147797 chr11:56147788-56147797 chr11:56147788-56147797
8	CEBPB	chr11:56111917-56111963	A549	lung:	n/a	n/a
9	CEBPB	chr11:56138112-56138329	HepG2	liver:	n/a	chr11:56138266-56138277
10	CEBPB	chr11:56147604-56147989	IMR90	lung:	n/a	chr11:56147786-56147799 chr11:56147786-56147797 chr11:56147786-56147799 chr11:56147788-56147797 chr11:56147788-56147797 chr11:56147788-56147797
11	CEBPB	chr11:56213754-56213902	A549	lung:	n/a	n/a
12	CEBPB	chr11:56156453-56156716	HepG2	liver:	n/a	n/a
13	CEBPB	chr11:56171906-56172267	HepG2	liver:	n/a	chr11:56172088-56172099
14	CEBPB	chr11:56173447-56173559	A549	lung:	n/a	n/a
15	CEBPB	chr11:56199056-56199115	A549	lung:	n/a	n/a
16	CEBPB	chr11:56147589-56147981	K562	blood:	n/a	chr11:56147786-56147799 chr11:56147786-56147797 chr11:56147786-56147799 chr11:56147788-56147797 chr11:56147788-56147797 chr11:56147788-56147797
17	CEBPB	chr11:56138128-56138346	A549	lung:	n/a	chr11:56138266-56138277
18	CEBPB	chr11:56111830-56112110	HepG2	liver:	n/a	chr11:56111955-56111968 chr11:56111955-56111966 chr11:56111957-56111968 chr11:56111955-56111968 chr11:56111957-56111968 chr11:56111955-56111968
19	CEBPB	chr11:56156547-56156579	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr11:56168366-56168512	MCF-7	breast:	n/a	n/a
21	CTCF	chr11:56128090-56128173	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr11:56168372-56168507	MCF-7	breast:	n/a	n/a
23	CTCF	chr11:56163680-56163718	A549	lung:	n/a	n/a
24	CTCF	chr11:56163840-56163990	A549	lung:	n/a	n/a
25	CTCF	chr11:56163700-56163850	A549	lung:	n/a	chr11:56163712-56163730 chr11:56163707-56163728
26	CTCF	chr11:56163600-56163750	HepG2	liver:	n/a	chr11:56163712-56163730 chr11:56163707-56163728
27	CTCF	chr11:56168356-56168512	MCF-7	breast:	n/a	n/a
28	CTCF	chr11:56163580-56163730	SK-N-SH_RA	brain:	n/a	chr11:56163712-56163730 chr11:56163707-56163728
29	CTCF	chr11:56167131-56167206	LNCaP	prostate:	n/a	n/a
30	CTCF	chr11:56163840-56163990	K562	blood:	n/a	n/a
31	CTCF	chr11:56163640-56163790	WERI-Rb-1	eye:	n/a	chr11:56163712-56163730 chr11:56163707-56163728
32	CTCF	chr11:56163600-56163750	MCF-7	breast:	n/a	chr11:56163712-56163730 chr11:56163707-56163728
33	CTCF	chr11:56163586-56163805	H1-hESC	embryonic stem cell:	n/a	chr11:56163712-56163730 chr11:56163707-56163728
34	CTCF	chr11:56112640-56112790	GM12865	blood:	n/a	n/a
35	CTCF	chr11:56120920-56121070	Caco-2	colon:	n/a	n/a
36	CTCF	chr11:56216924-56216965	LNCaP	prostate:	n/a	n/a
37	CTCF	chr11:56163640-56163790	GM12875	blood:	n/a	chr11:56163712-56163730 chr11:56163707-56163728
38	CTCF	chr11:56168357-56168510	Fibrobl	skin:	n/a	n/a
39	CTCF	chr11:56163640-56163790	HEK293	kidney:	n/a	chr11:56163712-56163730 chr11:56163707-56163728
40	CTCF	chr11:56168439-56168490	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr11:56163653-56163782	MCF-7	breast:	n/a	chr11:56163712-56163730 chr11:56163707-56163728
42	CTCF	chr11:56216892-56216933	ProgFib	skin:	n/a	n/a
43	CTCF	chr11:56098675-56098716	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr11:56168362-56168509	NHEK	skin:	n/a	n/a
45	CTCF	chr11:56163607-56163820	LNCaP	prostate:	n/a	chr11:56163712-56163730 chr11:56163707-56163728
46	CTCF	chr11:56163644-56163776	Gliobla	brain:	n/a	chr11:56163712-56163730 chr11:56163707-56163728
47	CTCF	chr11:56094415-56094473	Fibrobl	skin:	n/a	n/a
48	CTCF	chr11:56163640-56163790	MCF-7	breast:	n/a	chr11:56163712-56163730 chr11:56163707-56163728
49	CTCF	chr11:56163820-56163970	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr11:56206050-56206156	ProgFib	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:56113543-56113593	HRE	kidney:	n/a
2	chr11:56112384-56112434	MCF10A-Er-Src	breast:	n/a
3	chr11:56086656-56086706	HCT-116	colon:	n/a
4	chr11:56113543-56113593	MCF-7	breast:	n/a
5	chr11:56113543-56113593	T-47D	breast:	n/a
6	chr11:56113543-56113593	HNPCEpiC	eye:	n/a
7	chr11:56113543-56113593	HIPEpiC	eye:	n/a
8	chr11:56112153-56112203	NHDF-neo	bronchial:	n/a
9	chr11:56085745-56085795	GM12892	blood:	n/a
10	chr11:56099655-56099705	ProgFib	skin:	n/a
11	chr11:56099798-56099848	AG09309	skin:	n/a
12	chr11:56113768-56113818	AoSMC	blood vessel:	n/a
13	chr11:56143818-56143868	HPAEpiC	pulmonary alveolar:	n/a
14	chr11:56113543-56113593	NHDF-neo	bronchial:	n/a
15	chr11:56113768-56113818	HEEpiC	esophagus:	n/a
16	chr11:56112384-56112434	SK-N-MC	brain:	n/a
17	chr11:56143818-56143868	CMK	blood:	n/a
18	chr11:56099655-56099705	HEEpiC	esophagus:	n/a
19	chr11:56112384-56112434	IMR90	lung:	fetal
20	chr11:56099968-56100018	HAEpiC	amniotic membrane:	n/a
21	chr11:56112384-56112434	GM19239	blood:	n/a
22	chr11:56128137-56128187	GM19239	blood:	n/a
23	chr11:56143818-56143868	HCPEpiC	choroid plexus:	n/a
24	chr11:56086656-56086706	HPAEpiC	pulmonary alveolar:	n/a
25	chr11:56128137-56128187	BE2_C	brain:	n/a
26	chr11:56112153-56112203	GM12891	blood:	n/a
27	chr11:56230456-56230506	SK-N-SH_RA	brain:	n/a
28	chr11:56113543-56113593	SAEC	small airway:	n/a
29	chr11:56099798-56099848	MCF10A-Er-Src	breast:	n/a
30	chr11:56230456-56230506	AoSMC	blood vessel:	n/a
31	chr11:56112153-56112203	GM19239	blood:	n/a
32	chr11:56099968-56100018	HIPEpiC	eye:	n/a
33	chr11:56185737-56185787	PFSK-1	brain:	n/a
34	chr11:56085425-56085475	ECC-1	luminal epithelium:	n/a
35	chr11:56113543-56113593	HAEpiC	amniotic membrane:	n/a
36	chr11:56141839-56141889	NH-A	brain:	n/a
37	chr11:56085745-56085795	NT2-D1	testis:	n/a
38	chr11:56230456-56230506	HAEpiC	amniotic membrane:	n/a
39	chr11:56185737-56185787	CMK	blood:	n/a
40	chr11:56085425-56085475	NHBE	bronchial:	n/a
41	chr11:56185228-56185278	ovcar-3	ovarian:	n/a
42	chr11:56112384-56112434	HAEpiC	amniotic membrane:	n/a
43	chr11:56113543-56113593	PFSK-1	brain:	n/a
44	chr11:56112153-56112203	U87	brain:	n/a
45	chr11:56143818-56143868	BJ	skin:	n/a
46	chr11:56185737-56185787	HAEpiC	amniotic membrane:	n/a
47	chr11:56086656-56086706	ECC-1	luminal epithelium:	n/a
48	chr11:56112153-56112203	HCM	heart:	n/a
49	chr11:56099968-56100018	NHDF-neo	bronchial:	n/a
50	chr11:56113543-56113593	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:56181160..56181939-chr6:137746651..137747385,2	MCF-7	breast:
2	chr11:56127160..56128874-chr11:56130489..56132638,2	K562	blood:
3	chr11:56082649..56084354-chr11:56114300..56117003,2	K562	blood:

Variant related genes	Relation type
RPL5P29	TF binding region
OR8U1	TF binding region
OR5M4P	TF binding region
OR8K3	TF binding region
FAM8A2P	TF binding region
OR8K2P	TF binding region
OR8L1P	TF binding region
OR5R1	TF binding region
ENSG00000272987	TF binding region
OR5AL2P	TF binding region
OR8J1	TF binding region
OR5AL1	TF binding region
OR5M9	TF binding region
OR8K1	TF binding region
RPL5P29	CpG island
OR8U1	CpG island
OR5M4P	CpG island
OR8K3	CpG island
FAM8A2P	CpG island
OR8K2P	CpG island
OR8L1P	CpG island
OR5R1	CpG island
ENSG00000272987	CpG island
OR5AL2P	CpG island
OR8J1	CpG island
OR5AL1	CpG island
OR5M9	CpG island
OR8K1	CpG island
ENSG00000172487	chromatin interactions

Extended variants
information (count: 1283 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567456717	chr11:56084639-56084640	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs192013046	chr11:56084646-56084647	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs539837206	chr11:56084738-56084739	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs563328654	chr11:56084762-56084763	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs183869676	chr11:56084781-56084782	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs577047085	chr11:56084799-56084800	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs575292344	chr11:56085444-56085445	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs368080695	chr11:56085754-56085755	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs373497071	chr11:56085762-56085763	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs566814228	chr11:56085775-56085776	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs561014483	chr11:56094409-56094410	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs75503824	chr11:56094525-56094526	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs188353261	chr11:56094528-56094529	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs192591991	chr11:56094530-56094531	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs75258208	chr11:56094565-56094566	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs78885536	chr11:56094623-56094624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565907347	chr11:56094628-56094629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536427779	chr11:56094719-56094720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554900785	chr11:56094733-56094734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374858021	chr11:56094742-56094743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183655832	chr11:56094749-56094750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148376815	chr11:56094762-56094763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141600273	chr11:56094777-56094778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577316733	chr11:56094972-56094973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551876117	chr11:56094976-56094977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187975781	chr11:56094977-56094978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs150332367	chr11:56094981-56094982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs78121867	chr11:56094987-56094988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs199637554	chr11:56095094-56095095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs61903478	chr11:56095152-56095153	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs542799694	chr11:56095208-56095209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568114011	chr11:56095225-56095226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560974608	chr11:56095237-56095238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531392950	chr11:56095247-56095248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543165673	chr11:56095248-56095249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs11227917	chr11:56095322-56095323	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs532002863	chr11:56095327-56095328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs111872101	chr11:56095337-56095338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs566018756	chr11:56095345-56095346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547253582	chr11:56095350-56095351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530366764	chr11:56095428-56095429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139480386	chr11:56095447-56095448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs180835519	chr11:56095460-56095461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537510877	chr11:56095466-56095467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559106880	chr11:56095477-56095478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566555378	chr11:56095478-56095479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547857509	chr11:56095490-56095491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs56223672	chr11:56095492-56095493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570828691	chr11:56095514-56095515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184836601	chr11:56095527-56095528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	17142309	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:56094400-56094600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
2	chr11:56094600-56095800	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr11:56097200-56104800	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr11:56099400-56099800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr11:56100800-56101200	Active TSS	Brain Hippocampus Middle	brain
6	chr11:56101000-56101400	Enhancers	Brain Cingulate Gyrus	brain
7	chr11:56104400-56105400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
8	chr11:56104600-56105200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr11:56104800-56105200	Enhancers	H1 Cell Line	embryonic stem cell
10	chr11:56104800-56105400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr11:56105000-56105200	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr11:56105000-56105200	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr11:56105000-56105400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
14	chr11:56105200-56105400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr11:56105200-56105400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr11:56105200-56105600	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr11:56105400-56105600	Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr11:56105400-56105600	Active TSS	iPS-20b Cell Line	embryonic stem cell
19	chr11:56111800-56112400	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr11:56111800-56112600	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr11:56112000-56112400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr11:56112200-56112800	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr11:56124600-56125200	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr11:56143200-56143800	Active TSS	Brain Substantia Nigra	brain
25	chr11:56156200-56157000	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr11:56161200-56162800	Enhancers	Fetal Intestine Small	intestine
27	chr11:56161200-56163000	Enhancers	Fetal Intestine Large	intestine
28	chr11:56163600-56164000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr11:56169600-56170000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr11:56171000-56172400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr11:56171600-56172400	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr11:56173600-56173800	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr11:56173800-56175400	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr11:56200400-56200800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr11:56210000-56210800	Enhancers	Fetal Intestine Large	intestine
36	chr11:56210800-56211000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr11:56210800-56211200	Weak transcription	Fetal Intestine Large	intestine
38	chr11:56211200-56211600	Enhancers	Fetal Intestine Large	intestine
39	chr11:56220800-56221800	Enhancers	Fetal Brain Male	brain
40	chr11:56222400-56222800	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr11:56223400-56224200	Enhancers	HUES48 Cell Line	embryonic stem cell

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