Variant report

Variant	nsv889146
Chromosome Location	chr7:124996787-125083020
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:301)
CpG islands
(count:0)
Chromatin interactive
region (count:15)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:301 , 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	chr7:125036847-125037232	K562	blood:	n/a	n/a
2	ATF1	chr7:125036628-125037136	K562	blood:	n/a	n/a
3	ATF3	chr7:125036857-125037111	K562	blood:	n/a	n/a
4	BHLHE40	chr7:125052988-125053632	GM12878	blood:	n/a	n/a
5	CEBPB	chr7:125021399-125021663	IMR90	lung:	n/a	n/a
6	CEBPB	chr7:125013215-125013415	HepG2	liver:	n/a	chr7:125013342-125013353 chr7:125013340-125013353 chr7:125013340-125013351 chr7:125013340-125013353 chr7:125013340-125013353
7	CEBPB	chr7:125010980-125011205	A549	lung:	n/a	chr7:125011072-125011083
8	CEBPB	chr7:125010917-125011228	HepG2	liver:	n/a	chr7:125011072-125011083
9	CEBPB	chr7:125013289-125013418	K562	blood:	n/a	chr7:125013342-125013353 chr7:125013340-125013353 chr7:125013340-125013351 chr7:125013340-125013353 chr7:125013340-125013353
10	CEBPD	chr7:125036863-125037248	K562	blood:	n/a	n/a
11	CHD2	chr7:125053474-125053659	GM12878	blood:	n/a	n/a
12	CREB1	chr7:125063828-125064124	GM12878	blood:	n/a	n/a
13	CTCF	chr7:125023489-125023615	GM10248	blood:	n/a	n/a
14	CTCF	chr7:125023513-125023661	K562	blood:	n/a	n/a
15	CTCF	chr7:125076380-125076530	HRE	kidney:	n/a	n/a
16	CTCF	chr7:125023420-125023570	GM12873	blood:	n/a	n/a
17	CTCF	chr7:125023460-125023610	MCF-7	breast:	n/a	n/a
18	CTCF	chr7:125023460-125023610	GM12872	blood:	n/a	n/a
19	CTCF	chr7:125023537-125023631	GM10266	blood:	n/a	n/a
20	CTCF	chr7:125023501-125023661	GM13977	blood:	n/a	n/a
21	CTCF	chr7:125023532-125023607	MCF-7	breast:	n/a	n/a
22	CTCF	chr7:125023480-125023630	GM12866	blood:	n/a	n/a
23	CTCF	chr7:125023460-125023610	GM12869	blood:	n/a	n/a
24	CTCF	chr7:125023540-125023690	GM12874	blood:	n/a	n/a
25	CTCF	chr7:125023560-125023710	A549	lung:	n/a	n/a
26	CTCF	chr7:125023520-125023670	SAEC	small airway:	n/a	n/a
27	CTCF	chr7:125023440-125023590	HAc	cerebellar:	n/a	n/a
28	CTCF	chr7:125023440-125023590	K562	blood:	n/a	n/a
29	CTCF	chr7:125023480-125023630	HepG2	liver:	n/a	n/a
30	CTCF	chr7:125023540-125023690	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr7:125003940-125004090	HCFaa	heart:	n/a	n/a
32	CTCF	chr7:125023440-125023590	GM12865	blood:	n/a	n/a
33	CTCF	chr7:125023500-125023650	BE2_C	brain:	n/a	n/a
34	CTCF	chr7:125004100-125004250	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr7:125023462-125023650	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr7:125023520-125023670	HRE	kidney:	n/a	n/a
37	CTCF	chr7:125023440-125023590	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr7:125023500-125023650	SAEC	small airway:	n/a	n/a
39	CTCF	chr7:125008200-125008350	K562	blood:	n/a	n/a
40	CTCF	chr7:125023480-125023630	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr7:125023480-125023630	HMEC	breast:	n/a	n/a
42	CTCF	chr7:125004020-125004170	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr7:125023500-125023650	GM12874	blood:	n/a	n/a
44	CTCF	chr7:125023460-125023610	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr7:125023484-125023649	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr7:125023440-125023590	GM06990	blood:	n/a	n/a
47	CTCF	chr7:125023516-125023631	HepG2	liver:	n/a	n/a
48	CTCF	chr7:125003920-125004070	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr7:125023460-125023610	HepG2	liver:	n/a	n/a
50	CTCF	chr7:125023480-125023630	HCT-116	colon:	n/a	n/a

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:125037857..125040245-chr7:125044740..125047619,2	K562	blood:
2	chr7:125044926..125048888-chr7:125049294..125054485,5	K562	blood:
3	chr7:124699558..124701618-chr7:125055753..125057701,2	K562	blood:
4	chr7:125037857..125040245-chr7:125044740..125047619,2	K562	blood:
5	chr7:125014089..125016137-chr7:125017840..125020682,3	K562	blood:
6	chr7:125070959..125073239-chr7:125075739..125078658,3	K562	blood:
7	chr3:108533640..108534622-chr7:125014752..125015433,2	MCF-7	breast:
8	chr7:125070959..125073239-chr7:125075739..125078658,3	K562	blood:
9	chr7:125003566..125005765-chr7:125027328..125029861,2	K562	blood:
10	chr7:125014089..125016137-chr7:125017840..125020682,3	K562	blood:
11	chr7:125023517..125024026-chr7:125310752..125311652,2	MCF-7	breast:
12	chr7:125044926..125048888-chr7:125049294..125054485,5	K562	blood:
13	chr7:125003566..125005765-chr7:125027328..125029861,2	K562	blood:
14	chr7:123483979..123486169-chr7:125020238..125022477,2	K562	blood:
15	chr7:124965414..124966985-chr7:125006930..125009873,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPAM1-5	chr7:125003489-125003570	ENSG00000237764.2
2	lnc-SPAM1-5	chr7:125019112-125019375	ENSG00000237764.2
3	lnc-SPAM1-5	chr7:125019112-125019375	NR_110188
4	lnc-SPAM1-6	chr7:125078165-125078351	ENSG00000227869
5	lnc-SPAM1-6	chr7:125078276-125078351	ENSG00000227869
6	lnc-SPAM1-6	chr7:125071401-125071647	NONHSAT123109
7	lnc-SPAM1-5	chr7:125019112-125019375	NONHSAT123102
8	lnc-SPAM1-6	chr7:125071401-125071647	ENSG00000227869
9	lnc-SPAM1-5	chr7:125003489-125003570	NR_110188
10	lnc-SPAM1-6	chr7:125078165-125078351	NONHSAT123109
11	lnc-SPAM1-5	chr7:125003489-125003570	NONHSAT123102
12	lnc-SPAM1-6	chr7:125078199-125078351	ENSG00000227869

No data

Variant related genes	Relation type
ENSG00000227869	TF binding region
ENSG00000227869	chromatin interactions
ENSG00000106302	chromatin interactions

Extended variants
information (count: 2605 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2605 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11981796	chr7:124996787-124996788	Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs577054396	chr7:124996803-124996804	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551782867	chr7:124996832-124996833	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs571538076	chr7:124996854-124996855	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537410906	chr7:124996859-124996860	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562885546	chr7:124996872-124996873	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531783620	chr7:124996880-124996881	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs74748557	chr7:124997057-124997058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs114818417	chr7:124997080-124997081	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs527605807	chr7:124997083-124997084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556520148	chr7:124997117-124997118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569919358	chr7:124997216-124997217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546854674	chr7:124997217-124997218	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570744829	chr7:124997225-124997226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs35349677	chr7:124997262-124997263	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192108274	chr7:124997307-124997308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs535657613	chr7:124997310-124997311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375387788	chr7:124997340-124997341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs151094203	chr7:124997417-124997418	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs73719388	chr7:124997422-124997423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535494739	chr7:124997423-124997424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs4728021	chr7:124997432-124997433	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs28409697	chr7:124997436-124997437	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs147047305	chr7:124997448-124997449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572151726	chr7:124997451-124997452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555549819	chr7:124997454-124997455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201797167	chr7:124997503-124997504	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557768279	chr7:124997542-124997543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183836888	chr7:124997577-124997578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577116482	chr7:124997606-124997607	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140762427	chr7:124997636-124997637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs74951873	chr7:124997641-124997642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576474466	chr7:124997642-124997643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113762919	chr7:124997667-124997668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188711313	chr7:124997697-124997698	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527721393	chr7:124997706-124997707	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150122339	chr7:124997733-124997734	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs138374915	chr7:124997754-124997755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79147332	chr7:124997758-124997759	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569800243	chr7:124997826-124997827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs180888751	chr7:124997836-124997837	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549092584	chr7:124997890-124997891	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565425814	chr7:124997892-124997893	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs368584714	chr7:124997894-124997895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534360810	chr7:124998089-124998090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs1346365	chr7:124998105-124998106	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs961763	chr7:124998118-124998119	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs6956056	chr7:124998120-124998121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556500653	chr7:124998136-124998137	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576603780	chr7:124998158-124998159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	21635232	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Autism	20858243	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:124995600-124999400	Enhancers	HUVEC	blood vessel
2	chr7:124995800-124996800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr7:124995800-124999000	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr7:124996000-124997000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr7:124996400-124997600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr7:124996600-124997000	Weak transcription	NH-A	brain
7	chr7:124996800-124997800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr7:124997000-124997200	Enhancers	NH-A	brain
9	chr7:124997000-124999000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr7:124997200-125003800	Weak transcription	NH-A	brain
11	chr7:124997400-124999000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr7:124997600-124998400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr7:124997800-124998000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr7:125003800-125004400	Enhancers	NH-A	brain
15	chr7:125004800-125005000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr7:125015400-125016400	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr7:125015400-125017000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr7:125015800-125017200	Enhancers	Brain Germinal Matrix	brain
19	chr7:125021400-125023800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr7:125023800-125028000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr7:125028000-125029000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr7:125029000-125031000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr7:125031000-125031200	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr7:125031000-125031400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr7:125031200-125032400	Enhancers	HUVEC	blood vessel
26	chr7:125031200-125036200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr7:125032200-125032400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr7:125034200-125034400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr7:125034200-125034400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr7:125034600-125035800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr7:125034600-125035800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr7:125035800-125036400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr7:125035800-125039200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr7:125035800-125039800	Enhancers	Primary hematopoietic stem cells	blood
35	chr7:125036200-125038600	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr7:125036400-125037600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr7:125036400-125037800	Enhancers	K562	blood
38	chr7:125037600-125039800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr7:125039000-125039800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr7:125039400-125039800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr7:125039400-125039800	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr7:125045400-125045600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr7:125045600-125050400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr7:125046200-125046600	Enhancers	HUVEC	blood vessel
45	chr7:125049600-125050400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr7:125049800-125050000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr7:125049800-125050600	Enhancers	HMEC	breast
48	chr7:125050000-125053600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr7:125050400-125050800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr7:125050400-125059600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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