Variant report

Variant	esv18042
Chromosome Location	chr1:173929654-173932522
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:23)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:23 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	GATA2	chr1:173929663-173929991	SH-SY5Y	brain:	n/a	n/a
2	GATA3	chr1:173929653-173930198	SH-SY5Y	brain:	n/a	n/a
3	GATA3	chr1:173931667-173931831	SH-SY5Y	brain:	n/a	n/a
4	GATA3	chr1:173930849-173930873	SH-SY5Y	brain:	n/a	n/a
5	HCFC1	chr1:173931428-173931673	K562	blood:	n/a	n/a
6	MAFF	chr1:173929819-173930153	K562	blood:	n/a	n/a
7	MAFK	chr1:173929844-173930174	Hela-S3	cervix:	n/a	n/a
8	MAFK	chr1:173929808-173930144	HepG2	liver:	n/a	n/a
9	MAFK	chr1:173929808-173930133	K562	blood:	n/a	n/a
10	MAFK	chr1:173929832-173930138	HepG2	liver:	n/a	n/a
11	MAFK	chr1:173929827-173930161	IMR90	lung:	n/a	n/a
12	MXI1	chr1:173929607-173930295	SK-N-SH	brain:	n/a	n/a
13	MYC	chr1:173931064-173931094	MCF-7	breast:	n/a	n/a
14	POLR2A	chr1:173931577-173931581	MCF-7	breast:	n/a	n/a
15	POLR2A	chr1:173931601-173931901	MCF-7	breast:	n/a	n/a
16	POLR2A	chr1:173931019-173931274	MCF-7	breast:	n/a	n/a
17	POLR2A	chr1:173931149-173931195	MCF-7	breast:	n/a	n/a
18	POLR2A	chr1:173932375-173932460	Hela-S3	cervix:	n/a	n/a
19	SIX5	chr1:173931437-173931607	K562	blood:	n/a	n/a
20	USF1	chr1:173929785-173930011	SK-N-SH_RA	brain:	n/a	n/a
21	USF1	chr1:173929806-173930094	SK-N-SH_RA	brain:	n/a	n/a
22	ZNF143	chr1:173931462-173931618	GM12878	blood:	n/a	n/a
23	ZNF143	chr1:173931420-173931714	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:173930183-173930233	HIPEpiC	eye:	n/a
2	chr1:173930183-173930233	A549	lung:	n/a
3	chr1:173930183-173930233	PFSK-1	brain:	n/a
4	chr1:173930183-173930233	HNPCEpiC	eye:	n/a
5	chr1:173930183-173930233	SKMC	muscle:	n/a
6	chr1:173930183-173930233	Hela-S3	cervix:	n/a
7	chr1:173930183-173930233	LNCaP	prostate:	n/a
8	chr1:173930183-173930233	Caco-2	colon:	n/a
9	chr1:173930183-173930233	PANC-1	pancreas:	n/a
10	chr1:173930183-173930233	AoSMC	blood vessel:	n/a
11	chr1:173930183-173930233	AG04450	lung:	fetal
12	chr1:173930183-173930233	NHBE	bronchial:	n/a
13	chr1:173930183-173930233	Jurkat	blood:	n/a
14	chr1:173930183-173930233	AG10803	skin:	n/a
15	chr1:173930183-173930233	GM06990	blood:	n/a
16	chr1:173930183-173930233	HEEpiC	esophagus:	n/a
17	chr1:173930183-173930233	AG04449	skin:	fetal
18	chr1:173930183-173930233	HCF	heart:	n/a
19	chr1:173930183-173930233	T-47D	breast:	n/a
20	chr1:173930183-173930233	HAEpiC	amniotic membrane:	n/a
21	chr1:173930183-173930233	SAEC	small airway:	n/a
22	chr1:173930183-173930233	IMR90	lung:	fetal
23	chr1:173930183-173930233	Hepatocyte	liver:	n/a
24	chr1:173930183-173930233	CMK	blood:	n/a
25	chr1:173930183-173930233	ovcar-3	ovarian:	n/a
26	chr1:173930183-173930233	HEK293	kidney:	embryo
27	chr1:173930183-173930233	SK-N-MC	brain:	n/a
28	chr1:173930183-173930233	GM19239	blood:	n/a
29	chr1:173930183-173930233	NB4	blood:	n/a
30	chr1:173930183-173930233	NHDF-neo	bronchial:	n/a
31	chr1:173930183-173930233	HCPEpiC	choroid plexus:	n/a
32	chr1:173930183-173930233	AG09309	skin:	n/a
33	chr1:173930183-173930233	HRE	kidney:	n/a
34	chr1:173930183-173930233	K562	blood:	n/a
35	chr1:173930183-173930233	HL-60	blood:	n/a
36	chr1:173930183-173930233	SK-N-SH	brain:	n/a
37	chr1:173930183-173930233	U87	brain:	n/a
38	chr1:173930183-173930233	AG09319	gingival:	n/a
39	chr1:173930183-173930233	NT2-D1	testis:	n/a
40	chr1:173930183-173930233	BJ	skin:	n/a
41	chr1:173930183-173930233	MCF10A-Er-Src	breast:	n/a
42	chr1:173930183-173930233	HRCEpiC	kidney:	n/a
43	chr1:173930183-173930233	PrEC	prostate:	n/a
44	chr1:173930183-173930233	GM12878	blood:	n/a
45	chr1:173930183-173930233	ProgFib	skin:	n/a
46	chr1:173930183-173930233	GM12892	blood:	n/a
47	chr1:173930183-173930233	SK-N-SH_RA	brain:	n/a
48	chr1:173930183-173930233	HMEC	breast:	n/a
49	chr1:173930183-173930233	BE2_C	brain:	n/a
50	chr1:173930183-173930233	NH-A	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:173929519..173931322-chr1:173931556..173934242,2	MCF-7	breast:
2	chr1:173835905..173838790-chr1:173929682..173932448,3	MCF-7	breast:
3	chr1:173931023..173932801-chr1:173933873..173936006,2	MCF-7	breast:
4	chr1:173931135..173933401-chr1:173937060..173938685,2	K562	blood:

No data

Variant related genes	Relation type
RC3H1	TF binding region
RC3H1	CpG island
ENSG00000135870	chromatin interactions
ENSG00000185278	chromatin interactions
ENSG00000234741	chromatin interactions
ENSG00000200755	chromatin interactions

Extended variants
information (count: 111 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:111 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534962769	chr1:173929667-173929668	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs372683159	chr1:173929669-173929670	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576941678	chr1:173929702-173929703	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs546038439	chr1:173929728-173929729	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs7413166	chr1:173929735-173929736	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs78760256	chr1:173929779-173929780	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs577786730	chr1:173929870-173929871	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs542231896	chr1:173929895-173929896	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs12063296	chr1:173929899-173929900	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs530884738	chr1:173929943-173929944	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs368225334	chr1:173929969-173929970	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs1407597	chr1:173929988-173929989	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs532749008	chr1:173929989-173929990	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs75814656	chr1:173929999-173930000	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs192459503	chr1:173930003-173930004	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs145189635	chr1:173930010-173930011	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs546792587	chr1:173930015-173930016	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs547006043	chr1:173930038-173930039	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs528172040	chr1:173930043-173930044	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs546132150	chr1:173930047-173930048	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs568076349	chr1:173930099-173930100	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs536672412	chr1:173930122-173930123	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs550617507	chr1:173930150-173930151	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs368557511	chr1:173930164-173930165	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs570465744	chr1:173930168-173930169	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs184799841	chr1:173930217-173930218	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs201261578	chr1:173930219-173930220	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs140858270	chr1:173930222-173930223	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs201050903	chr1:173930248-173930249	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs373306163	chr1:173930272-173930273	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs377588868	chr1:173930274-173930275	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs535773915	chr1:173930317-173930318	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs555394791	chr1:173930358-173930359	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs575558704	chr1:173930362-173930363	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs140937934	chr1:173930366-173930367	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs144597354	chr1:173930379-173930380	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs548271300	chr1:173930448-173930449	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs564556533	chr1:173930456-173930457	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs577763908	chr1:173930487-173930488	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs114730434	chr1:173930498-173930499	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs187962087	chr1:173930539-173930540	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs368057471	chr1:173930604-173930605	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs144618049	chr1:173930611-173930612	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs549626008	chr1:173930634-173930635	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs146654584	chr1:173930637-173930638	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs200060720	chr1:173930699-173930700	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs530487127	chr1:173930701-173930702	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs572829728	chr1:173930702-173930703	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs191994294	chr1:173930732-173930733	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs539572066	chr1:173930811-173930812	Weak transcription Strong transcription Genic enhancers	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:205 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:173899800-173953800	Strong transcription	Primary T cells fromperipheralblood	blood
2	chr1:173900000-173958600	Strong transcription	Rectal Mucosa Donor 31	rectum
3	chr1:173900000-173962400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr1:173900000-173966600	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr1:173900000-173968200	Strong transcription	Primary monocytes fromperipheralblood	blood
6	chr1:173900200-173966400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr1:173900400-173964600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr1:173900800-173963800	Strong transcription	Primary T helper cells fromperipheralblood	blood
9	chr1:173901200-173931400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:173901400-173962200	Strong transcription	Duodenum Mucosa	Duodenum
11	chr1:173901600-173966400	Strong transcription	Primary neutrophils fromperipheralblood	blood
12	chr1:173901600-173966400	Strong transcription	Dnd41	blood
13	chr1:173902200-173954600	Strong transcription	Primary B cells from peripheral blood	blood
14	chr1:173902600-173954400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
15	chr1:173904000-173966400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:173904800-173954200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:173905000-173938400	Strong transcription	HUES6 Cell Line	embryonic stem cell
18	chr1:173905000-173962400	Strong transcription	HUES48 Cell Line	embryonic stem cell
19	chr1:173905200-173954600	Strong transcription	HUES64 Cell Line	embryonic stem cell
20	chr1:173906000-173940400	Strong transcription	Adipose Nuclei	Adipose
21	chr1:173906000-173959000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr1:173906200-173937600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr1:173906400-173931800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr1:173906800-173959000	Strong transcription	Liver	Liver
25	chr1:173909800-173974200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr1:173910200-173933600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr1:173910400-173952200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr1:173913000-173930200	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr1:173913400-173930800	Weak transcription	Psoas Muscle	Psoas
30	chr1:173915600-173977800	Weak transcription	Stomach Mucosa	stomach
31	chr1:173915800-173930200	Weak transcription	Right Ventricle	heart
32	chr1:173916000-173929800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr1:173916800-173929800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr1:173916800-173930400	Weak transcription	Aorta	Aorta
35	chr1:173917200-173929800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr1:173919600-173929800	Weak transcription	Brain Hippocampus Middle	brain
37	chr1:173920600-173930800	Weak transcription	Colonic Mucosa	Colon
38	chr1:173921400-173929800	Weak transcription	NHEK	skin
39	chr1:173922000-173932400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr1:173922200-173942000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr1:173922200-173954000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr1:173922400-173931400	Strong transcription	Fetal Intestine Small	intestine
43	chr1:173922400-173932000	Strong transcription	Fetal Stomach	stomach
44	chr1:173922600-173936400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr1:173923200-173931400	Strong transcription	Hela-S3	cervix
46	chr1:173923400-173954400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
47	chr1:173923400-173962400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr1:173923600-173939800	Strong transcription	H1 Cell Line	embryonic stem cell
49	chr1:173923800-173953800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr1:173923800-173954400	Strong transcription	iPS-20b Cell Line	embryonic stem cell

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