Variant report

Variant	esv3692957
Chromosome Location	chr1:173960747-173967521
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	EP300	chr1:173967193-173967486	SK-N-SH_RA	brain:	n/a	n/a
2	FOS	chr1:173964636-173964948	HUVEC	blood vessel:	n/a	chr1:173964798-173964808 chr1:173964797-173964808 chr1:173964798-173964808 chr1:173964798-173964807 chr1:173964798-173964808 chr1:173964798-173964808
3	FOS	chr1:173966211-173966384	MCF10A-Er-Src	breast:	n/a	n/a
4	FOS	chr1:173964706-173964942	MCF10A-Er-Src	breast:	n/a	chr1:173964798-173964808 chr1:173964797-173964808 chr1:173964798-173964808 chr1:173964798-173964807 chr1:173964798-173964808 chr1:173964798-173964808
5	FOS	chr1:173964701-173964942	MCF10A-Er-Src	breast:	n/a	chr1:173964798-173964808 chr1:173964797-173964808 chr1:173964798-173964808 chr1:173964798-173964807 chr1:173964798-173964808 chr1:173964798-173964808
6	FOS	chr1:173964685-173964901	MCF10A-Er-Src	breast:	n/a	chr1:173964798-173964808 chr1:173964797-173964808 chr1:173964798-173964808 chr1:173964798-173964807 chr1:173964798-173964808 chr1:173964798-173964808
7	FOS	chr1:173964636-173964963	MCF10A-Er-Src	breast:	n/a	chr1:173964798-173964808 chr1:173964797-173964808 chr1:173964798-173964808 chr1:173964798-173964807 chr1:173964798-173964808 chr1:173964798-173964808
8	GATA3	chr1:173967350-173967722	SH-SY5Y	brain:	n/a	n/a
9	GATA3	chr1:173966768-173967487	SK-N-SH	brain:	n/a	n/a
10	JUND	chr1:173964725-173964897	HepG2	liver:	n/a	chr1:173964798-173964808 chr1:173964798-173964808 chr1:173964798-173964807 chr1:173964797-173964808 chr1:173964798-173964808 chr1:173964798-173964808
11	JUND	chr1:173965387-173965622	HepG2	liver:	n/a	chr1:173965454-173965463
12	KAP1	chr1:173966364-173967096	K562	blood:	n/a	n/a
13	MAFK	chr1:173967173-173967337	HepG2	liver:	n/a	chr1:173967264-173967278 chr1:173967261-173967277
14	PAX5	chr1:173966199-173966435	GM12891	blood:	n/a	n/a
15	PAX5	chr1:173966038-173966407	GM12891	blood:	n/a	n/a
16	PAX5	chr1:173966159-173966405	GM12878	blood:	n/a	n/a
17	PAX5	chr1:173966201-173966400	GM12878	blood:	n/a	n/a
18	POLR2A	chr1:173965517-173965802	GM12878	blood:	n/a	n/a
19	POLR2A	chr1:173967514-173967565	MCF-7	breast:	n/a	n/a
20	POLR2A	chr1:173963463-173963487	MCF-7	breast:	n/a	n/a
21	POLR2A	chr1:173966040-173966072	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr1:173963427-173963462	MCF-7	breast:	n/a	n/a
23	POLR2A	chr1:173963782-173963832	ProgFib	skin:	n/a	n/a
24	POLR2A	chr1:173961844-173961959	HepG2	liver:	n/a	n/a
25	POLR2A	chr1:173963315-173963348	MCF-7	breast:	n/a	n/a
26	POLR2A	chr1:173963586-173963825	GM12878	blood:	n/a	n/a
27	POLR2A	chr1:173961889-173961968	MCF-7	breast:	n/a	n/a
28	POLR2A	chr1:173961985-173961987	MCF-7	breast:	n/a	n/a
29	POLR2A	chr1:173964126-173964345	HepG2	liver:	n/a	n/a
30	POLR2A	chr1:173961447-173961581	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr1:173965618-173965777	K562	blood:	n/a	n/a
32	POLR2A	chr1:173963399-173963423	MCF-7	breast:	n/a	n/a
33	RFX5	chr1:173961036-173961056	K562	blood:	n/a	n/a
34	STAT3	chr1:173966912-173967098	MCF10A-Er-Src	breast:	n/a	n/a
35	STAT3	chr1:173964823-173964899	MCF10A-Er-Src	breast:	n/a	n/a
36	ZNF384	chr1:173962036-173962057	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:173966344-173966394	HAEpiC	amniotic membrane:	n/a
2	chr1:173966344-173966394	HMEC	breast:	n/a
3	chr1:173961904-173961954	HEK293	kidney:	embryo
4	chr1:173966344-173966394	PFSK-1	brain:	n/a
5	chr1:173966344-173966394	AG09319	gingival:	n/a
6	chr1:173961904-173961954	AG09309	skin:	n/a
7	chr1:173961904-173961954	HRPEpiC	eye:	n/a
8	chr1:173966344-173966394	HRPEpiC	eye:	n/a
9	chr1:173961904-173961954	PFSK-1	brain:	n/a
10	chr1:173966344-173966394	HCM	heart:	n/a
11	chr1:173966344-173966394	U87	brain:	n/a
12	chr1:173961904-173961954	HCF	heart:	n/a
13	chr1:173961904-173961954	ECC-1	luminal epithelium:	n/a
14	chr1:173961904-173961954	LNCaP	prostate:	n/a
15	chr1:173961904-173961954	HEEpiC	esophagus:	n/a
16	chr1:173966344-173966394	HepG2	liver:	n/a
17	chr1:173966344-173966394	HIPEpiC	eye:	n/a
18	chr1:173966344-173966394	SKMC	muscle:	n/a
19	chr1:173961904-173961954	AoSMC	blood vessel:	n/a
20	chr1:173961904-173961954	GM06990	blood:	n/a
21	chr1:173966344-173966394	ovcar-3	ovarian:	n/a
22	chr1:173961904-173961954	HCPEpiC	choroid plexus:	n/a
23	chr1:173961904-173961954	SKMC	muscle:	n/a
24	chr1:173961904-173961954	NHBE	bronchial:	n/a
25	chr1:173961904-173961954	MCF10A-Er-Src	breast:	n/a
26	chr1:173961904-173961954	H1-hESC	embryonic stem cell:	embryo
27	chr1:173966344-173966394	AG04449	skin:	fetal
28	chr1:173966344-173966394	RPTEC	kidney:	n/a
29	chr1:173961904-173961954	SAEC	small airway:	n/a
30	chr1:173961904-173961954	ovcar-3	ovarian:	n/a
31	chr1:173961904-173961954	AG09319	gingival:	n/a
32	chr1:173961904-173961954	Hela-S3	cervix:	n/a
33	chr1:173966344-173966394	NB4	blood:	n/a
34	chr1:173966344-173966394	CMK	blood:	n/a
35	chr1:173961904-173961954	HAEpiC	amniotic membrane:	n/a
36	chr1:173966344-173966394	HCT-116	colon:	n/a
37	chr1:173961904-173961954	Caco-2	colon:	n/a
38	chr1:173961904-173961954	U87	brain:	n/a
39	chr1:173966344-173966394	AG10803	skin:	n/a
40	chr1:173966344-173966394	HEK293	kidney:	embryo
41	chr1:173961904-173961954	HRCEpiC	kidney:	n/a
42	chr1:173966344-173966394	GM12878	blood:	n/a
43	chr1:173966344-173966394	PANC-1	pancreas:	n/a
44	chr1:173966344-173966394	HPAEpiC	pulmonary alveolar:	n/a
45	chr1:173966344-173966394	HL-60	blood:	n/a
46	chr1:173961904-173961954	BE2_C	brain:	n/a
47	chr1:173966344-173966394	NHDF-neo	bronchial:	n/a
48	chr1:173966344-173966394	MCF10A-Er-Src	breast:	n/a
49	chr1:173966344-173966394	NT2-D1	testis:	n/a
50	chr1:173966344-173966394	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr1:173956360..173957903-chr1:173959725..173961914,2	K562	blood:
2	chr1:173959770..173961680-chr1:173990983..173993365,2	K562	blood:
3	chr1:173964310..173967666-chr1:173990049..173993050,6	MCF-7	breast:
4	chr1:173791607..173793893-chr1:173965038..173968720,3	K562	blood:
5	chr1:173835569..173838721-chr1:173965548..173969329,3	K562	blood:
6	chr1:173966661..173969075-chr1:173990133..173991820,3	MCF-7	breast:
7	chr1:173954538..173956167-chr1:173959585..173961567,2	K562	blood:
8	chr1:173966978..173969283-chr1:173971302..173973529,3	K562	blood:
9	chr1:173829121..173831364-chr1:173963945..173965806,2	MCF-7	breast:
10	chr1:173967156..173969283-chr1:173971628..173973529,2	K562	blood:
11	chr1:173964894..173966462-chr1:173970460..173973100,2	K562	blood:
12	chr1:173961254..173963664-chr1:173990369..173993312,2	MCF-7	breast:

Variant related genes	Relation type
RC3H1	TF binding region
RC3H1	CpG island
ENSG00000135870	chromatin interactions
ENSG00000185278	chromatin interactions
ENSG00000234741	chromatin interactions
ENSG00000117593	chromatin interactions
ENSG00000120334	chromatin interactions
ENSG00000224977	chromatin interactions

Extended variants
information (count: 240 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:240 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6425267	chr1:173960747-173960748	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs182306792	chr1:173960790-173960791	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs552325407	chr1:173960796-173960797	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs559545825	chr1:173960804-173960805	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs187870614	chr1:173960812-173960813	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs374072478	chr1:173960856-173960857	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs552907345	chr1:173960869-173960870	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs192635870	chr1:173960874-173960875	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs368091256	chr1:173960905-173960906	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs142449098	chr1:173961024-173961025	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs184462831	chr1:173961031-173961032	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs58183915	chr1:173961131-173961132	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs151195705	chr1:173961133-173961134	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs113218967	chr1:173961169-173961170	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs369491630	chr1:173961184-173961185	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs193178679	chr1:173961200-173961201	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs151028780	chr1:173961343-173961344	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs140902141	chr1:173961346-173961347	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs184621003	chr1:173961441-173961442	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs535698345	chr1:173961492-173961493	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs189893085	chr1:173961521-173961522	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs555739964	chr1:173961538-173961539	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs144494147	chr1:173961582-173961583	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs544594845	chr1:173961596-173961597	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs16846641	chr1:173961600-173961601	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs576912013	chr1:173961603-173961604	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs112523507	chr1:173961616-173961617	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs180682747	chr1:173961660-173961661	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs539585550	chr1:173961692-173961693	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs183796024	chr1:173961706-173961707	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs540524856	chr1:173961724-173961725	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs542033622	chr1:173961767-173961768	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs34709821	chr1:173961807-173961808	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs377599781	chr1:173961808-173961809	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs561817636	chr1:173961827-173961828	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs200607410	chr1:173961835-173961836	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs6425268	chr1:173961837-173961838	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs397981982	chr1:173961838-173961839	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs12754931	chr1:173961839-173961840	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
40	rs550621107	chr1:173961841-173961842	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs34315262	chr1:173961842-173961843	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs368010602	chr1:173961843-173961844	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs558441301	chr1:173961854-173961855	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs369273422	chr1:173961904-173961905	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs139661174	chr1:173961948-173961949	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs569006557	chr1:173961984-173961985	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs10912711	chr1:173961992-173961993	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs373378422	chr1:173962005-173962006	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs200436514	chr1:173962037-173962038	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs200335635	chr1:173962039-173962040	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20967226	CNVD
Autism	22495309	CNVD
Breast cancer	21611746	CNVD
Pancreatic cancer	17952125	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:173900000-173962400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr1:173900000-173966600	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr1:173900000-173968200	Strong transcription	Primary monocytes fromperipheralblood	blood
4	chr1:173900200-173966400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr1:173900400-173964600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr1:173900800-173963800	Strong transcription	Primary T helper cells fromperipheralblood	blood
7	chr1:173901400-173962200	Strong transcription	Duodenum Mucosa	Duodenum
8	chr1:173901600-173966400	Strong transcription	Primary neutrophils fromperipheralblood	blood
9	chr1:173901600-173966400	Strong transcription	Dnd41	blood
10	chr1:173904000-173966400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:173905000-173962400	Strong transcription	HUES48 Cell Line	embryonic stem cell
12	chr1:173909800-173974200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr1:173915600-173977800	Weak transcription	Stomach Mucosa	stomach
14	chr1:173923400-173962400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:173929000-173962200	Strong transcription	Rectal Mucosa Donor 29	rectum
16	chr1:173931200-173962400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr1:173931200-173962400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr1:173931200-173965600	Weak transcription	Small Intestine	intestine
19	chr1:173931200-173969800	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr1:173941000-173965000	Strong transcription	Fetal Thymus	thymus
21	chr1:173942200-173967400	Weak transcription	Fetal Heart	heart
22	chr1:173942200-173986200	Weak transcription	Fetal Brain Male	brain
23	chr1:173947000-173966000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr1:173949200-173970600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr1:173949600-173965600	Weak transcription	Esophagus	oesophagus
26	chr1:173949600-173970600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr1:173950200-173961800	Weak transcription	Aorta	Aorta
28	chr1:173950600-173973400	Weak transcription	Psoas Muscle	Psoas
29	chr1:173952200-173967200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr1:173952800-173962200	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr1:173952800-173967600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr1:173953200-173974200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr1:173954200-173961000	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr1:173954600-173963600	Strong transcription	Fetal Intestine Large	intestine
35	chr1:173955200-173962600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
36	chr1:173955200-173962800	Strong transcription	Primary T cells fromperipheralblood	blood
37	chr1:173955400-173962200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
38	chr1:173955600-173966200	Strong transcription	Primary B cells from peripheral blood	blood
39	chr1:173956000-173962200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr1:173956000-173962200	Strong transcription	Brain Germinal Matrix	brain
41	chr1:173956000-173962200	Strong transcription	Fetal Lung	lung
42	chr1:173956200-173962200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
43	chr1:173956200-173962600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr1:173956200-173963800	Strong transcription	Primary T helper cells PMA-I stimulated	--
45	chr1:173956200-173966400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr1:173956400-173962200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr1:173956400-173962200	Strong transcription	Fetal Kidney	kidney
48	chr1:173956400-173962600	Strong transcription	HUES64 Cell Line	embryonic stem cell
49	chr1:173956600-173962600	Strong transcription	HUES6 Cell Line	embryonic stem cell
50	chr1:173956600-173962600	Strong transcription	Primary hematopoietic stem cells	blood

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