Variant report

Variant	esv2764210
Chromosome Location	chr1:77825478-77838400
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	ATF1	chr1:77830671-77830692	K562	blood:	n/a	n/a
2	BACH1	chr1:77837156-77837175	K562	blood:	n/a	n/a
3	CEBPB	chr1:77837758-77838106	IMR90	lung:	n/a	chr1:77837934-77837945 chr1:77837936-77837945 chr1:77837936-77837947
4	CEBPB	chr1:77837853-77838011	K562	blood:	n/a	chr1:77837934-77837945 chr1:77837936-77837945 chr1:77837936-77837947
5	CEBPB	chr1:77836534-77837349	IMR90	lung:	n/a	chr1:77837107-77837119
6	CEBPB	chr1:77837826-77838026	HepG2	liver:	n/a	chr1:77837934-77837945 chr1:77837936-77837945 chr1:77837936-77837947
7	CTCF	chr1:77832506-77832525	GM13976	blood:	n/a	n/a
8	EP300	chr1:77836430-77837028	SK-N-SH_RA	brain:	n/a	chr1:77836438-77836454
9	EP300	chr1:77825952-77826334	SK-N-SH_RA	brain:	n/a	n/a
10	EP300	chr1:77836332-77837093	SK-N-SH	brain:	n/a	chr1:77836438-77836454
11	EP300	chr1:77825987-77826299	SK-N-SH_RA	brain:	n/a	n/a
12	EP300	chr1:77836420-77837040	SK-N-SH_RA	brain:	n/a	chr1:77836438-77836454
13	EP300	chr1:77836202-77837142	SK-N-SH	brain:	n/a	chr1:77836438-77836454
14	FOSL2	chr1:77836360-77837490	SK-N-SH	brain:	n/a	n/a
15	GATA3	chr1:77834280-77834443	SH-SY5Y	brain:	n/a	n/a
16	GATA3	chr1:77836257-77837264	SK-N-SH	brain:	n/a	chr1:77837163-77837171
17	GATA3	chr1:77836217-77837526	SK-N-SH	brain:	n/a	chr1:77837163-77837171 chr1:77837404-77837414 chr1:77837404-77837413 chr1:77837403-77837415 chr1:77837406-77837413 chr1:77837399-77837420 chr1:77837401-77837417
18	JUND	chr1:77829030-77829318	HepG2	liver:	n/a	n/a
19	JUND	chr1:77836231-77837224	SK-N-SH	brain:	n/a	n/a
20	JUND	chr1:77836366-77837470	SK-N-SH	brain:	n/a	n/a
21	MAFK	chr1:77836323-77837020	IMR90	lung:	n/a	n/a
22	MAX	chr1:77836328-77837046	SK-N-SH	brain:	n/a	n/a
23	MAX	chr1:77836250-77837074	SK-N-SH	brain:	n/a	n/a
24	MAX	chr1:77836618-77836996	NB4	blood:	n/a	n/a
25	NFIC	chr1:77836147-77837316	SK-N-SH	brain:	n/a	chr1:77836324-77836340
26	NFIC	chr1:77836250-77837086	SK-N-SH	brain:	n/a	chr1:77836324-77836340
27	NRF1	chr1:77832176-77832320	K562	blood:	n/a	n/a
28	PBX3	chr1:77836269-77837542	SK-N-SH	brain:	n/a	n/a
29	PBX3	chr1:77825931-77826318	SK-N-SH	brain:	n/a	n/a
30	PBX3	chr1:77836250-77837465	SK-N-SH	brain:	n/a	n/a
31	POLR2A	chr1:77831370-77831468	Gliobla	brain:	n/a	n/a
32	POLR2A	chr1:77829612-77829778	MCF10A-Er-Src	breast:	n/a	n/a
33	POLR2A	chr1:77831374-77831409	A549	lung:	n/a	n/a
34	POLR2A	chr1:77837220-77837289	MCF10A-Er-Src	breast:	n/a	n/a
35	POLR2A	chr1:77836642-77836880	ProgFib	skin:	n/a	n/a
36	POLR2A	chr1:77836404-77836938	SK-N-SH	brain:	n/a	n/a
37	POLR2A	chr1:77836461-77837059	SK-N-SH	brain:	n/a	n/a
38	POLR2A	chr1:77836439-77836537	ProgFib	skin:	n/a	n/a
39	POLR2A	chr1:77837925-77837976	ProgFib	skin:	n/a	n/a
40	POLR2A	chr1:77827936-77828046	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr1:77836910-77836990	ProgFib	skin:	n/a	n/a
42	POLR2A	chr1:77837857-77837868	ProgFib	skin:	n/a	n/a
43	POLR2A	chr1:77836644-77836957	U87	brain:	n/a	n/a
44	POLR2A	chr1:77837895-77837919	ProgFib	skin:	n/a	n/a
45	POLR2A	chr1:77835644-77835752	ProgFib	skin:	n/a	n/a
46	RAD21	chr1:77836498-77836957	SK-N-SH_RA	brain:	n/a	n/a
47	RAD21	chr1:77836337-77837023	SK-N-SH_RA	brain:	n/a	n/a
48	REST	chr1:77836643-77836991	SK-N-SH	brain:	n/a	n/a
49	REST	chr1:77836758-77837061	SK-N-SH	brain:	n/a	n/a
50	RFX5	chr1:77829221-77829338	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:77836400-77836450	HCT-116	colon:	n/a
2	chr1:77836400-77836450	GM06990	blood:	n/a
3	chr1:77836400-77836450	NH-A	brain:	n/a
4	chr1:77836400-77836450	PFSK-1	brain:	n/a
5	chr1:77836400-77836450	CMK	blood:	n/a
6	chr1:77836400-77836450	SK-N-SH_RA	brain:	n/a
7	chr1:77836400-77836450	SK-N-SH	brain:	n/a
8	chr1:77836400-77836450	ovcar-3	ovarian:	n/a
9	chr1:77836400-77836450	Caco-2	colon:	n/a
10	chr1:77836400-77836450	A549	lung:	n/a
11	chr1:77836400-77836450	PrEC	prostate:	n/a
12	chr1:77836400-77836450	H1-hESC	embryonic stem cell:	embryo
13	chr1:77836400-77836450	AG10803	skin:	n/a
14	chr1:77836400-77836450	HUVEC	blood vessel:	n/a
15	chr1:77836400-77836450	NHDF-neo	bronchial:	n/a
16	chr1:77836400-77836450	K562	blood:	n/a
17	chr1:77836400-77836450	AG04449	skin:	fetal
18	chr1:77836400-77836450	NHBE	bronchial:	n/a
19	chr1:77836400-77836450	AG09309	skin:	n/a
20	chr1:77836400-77836450	HAEpiC	amniotic membrane:	n/a
21	chr1:77836400-77836450	SAEC	small airway:	n/a
22	chr1:77836400-77836450	HEEpiC	esophagus:	n/a
23	chr1:77836400-77836450	HL-60	blood:	n/a
24	chr1:77836400-77836450	IMR90	lung:	fetal
25	chr1:77836400-77836450	HepG2	liver:	n/a
26	chr1:77836400-77836450	GM12878	blood:	n/a
27	chr1:77836400-77836450	RPTEC	kidney:	n/a
28	chr1:77836400-77836450	ECC-1	luminal epithelium:	n/a
29	chr1:77836400-77836450	HRCEpiC	kidney:	n/a
30	chr1:77836400-77836450	GM12892	blood:	n/a
31	chr1:77836400-77836450	HRPEpiC	eye:	n/a
32	chr1:77836400-77836450	SKMC	muscle:	n/a
33	chr1:77836400-77836450	Hepatocyte	liver:	n/a
34	chr1:77836400-77836450	LNCaP	prostate:	n/a
35	chr1:77836400-77836450	AG09319	gingival:	n/a
36	chr1:77836400-77836450	HCF	heart:	n/a
37	chr1:77836400-77836450	U87	brain:	n/a
38	chr1:77836400-77836450	SK-N-MC	brain:	n/a
39	chr1:77836400-77836450	HMEC	breast:	n/a
40	chr1:77836400-77836450	PANC-1	pancreas:	n/a
41	chr1:77836400-77836450	HPAEpiC	pulmonary alveolar:	n/a
42	chr1:77836400-77836450	HIPEpiC	eye:	n/a
43	chr1:77836400-77836450	GM12891	blood:	n/a
44	chr1:77836400-77836450	GM19239	blood:	n/a
45	chr1:77836400-77836450	T-47D	breast:	n/a
46	chr1:77836400-77836450	HRE	kidney:	n/a
47	chr1:77836400-77836450	NT2-D1	testis:	n/a
48	chr1:77836400-77836450	HCPEpiC	choroid plexus:	n/a
49	chr1:77836400-77836450	MCF-7	breast:	n/a
50	chr1:77836400-77836450	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:77838249..77841580-chr1:77844120..77846924,3	K562	blood:
2	chr1:77820213..77822574-chr1:77837980..77839971,2	K562	blood:
3	chr1:77817387..77819700-chr1:77829412..77831526,2	K562	blood:

Variant related genes	Relation type
AK5	TF binding region
AK5	CpG island

Extended variants
information (count: 507 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:507 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11162323	chr1:77825478-77825479	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550840839	chr1:77825620-77825621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536360312	chr1:77825643-77825644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142964093	chr1:77825651-77825652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs2815306	chr1:77825660-77825661	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs61783074	chr1:77825681-77825682	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs566405169	chr1:77825717-77825718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs72944755	chr1:77825752-77825753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs80284637	chr1:77825838-77825839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs576947699	chr1:77825847-77825848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs17100436	chr1:77825907-77825908	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs183465358	chr1:77825913-77825914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs150657702	chr1:77825924-77825925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs59559185	chr1:77825925-77825926	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs561374821	chr1:77825969-77825970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs17100440	chr1:77825996-77825997	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs535212899	chr1:77826033-77826034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs6681717	chr1:77826056-77826057	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs76674114	chr1:77826060-77826061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550900620	chr1:77826111-77826112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs562839274	chr1:77826149-77826150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs137993431	chr1:77826172-77826173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs115160075	chr1:77826176-77826177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs555474724	chr1:77826181-77826182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149477906	chr1:77826182-77826183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs570598228	chr1:77826226-77826227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563563566	chr1:77826252-77826253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538037070	chr1:77826272-77826273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs367935895	chr1:77826279-77826280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs114676891	chr1:77826300-77826301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs74986889	chr1:77826328-77826329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs72944757	chr1:77826332-77826333	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs536657827	chr1:77826333-77826334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs554972974	chr1:77826351-77826352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs369378414	chr1:77826353-77826354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs573166760	chr1:77826386-77826387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs143893233	chr1:77826432-77826433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs1869468	chr1:77826496-77826497	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs377315379	chr1:77826507-77826508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574672370	chr1:77826585-77826586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs115686023	chr1:77826618-77826619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs180997696	chr1:77826642-77826643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs35923030	chr1:77826688-77826689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs548451892	chr1:77826718-77826719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs10493604	chr1:77826732-77826733	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs527271752	chr1:77826745-77826746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs552034367	chr1:77826789-77826790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs186270639	chr1:77826795-77826796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs140286073	chr1:77826812-77826813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549965665	chr1:77826879-77826880	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:147 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77789000-77831200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:77795000-77836400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr1:77801000-77825800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:77803400-77839200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr1:77813800-77834200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr1:77814400-77835600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr1:77816200-77825800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr1:77817400-77834200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr1:77819800-77826800	Weak transcription	NHDF-Ad	bronchial
10	chr1:77819800-77835600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr1:77820400-77836400	Weak transcription	Primary T cells from cord blood	blood
12	chr1:77821000-77825600	Weak transcription	HSMMtube	muscle
13	chr1:77821000-77835600	Weak transcription	Brain Hippocampus Middle	brain
14	chr1:77821400-77825600	Weak transcription	HSMM	muscle
15	chr1:77822600-77825600	Weak transcription	Brain Cingulate Gyrus	brain
16	chr1:77824200-77825600	Weak transcription	Brain Angular Gyrus	brain
17	chr1:77824200-77825800	Weak transcription	Brain Substantia Nigra	brain
18	chr1:77824400-77836400	Weak transcription	Brain Anterior Caudate	brain
19	chr1:77825400-77826400	Enhancers	Muscle Satellite Cultured Cells	--
20	chr1:77825600-77825800	Enhancers	Brain Angular Gyrus	brain
21	chr1:77825600-77826000	Enhancers	Brain Cingulate Gyrus	brain
22	chr1:77825600-77826200	Enhancers	HSMMtube	muscle
23	chr1:77825600-77826800	Enhancers	HSMM	muscle
24	chr1:77825800-77826000	Enhancers	Brain Substantia Nigra	brain
25	chr1:77825800-77826200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:77825800-77826400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr1:77826200-77834200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr1:77826200-77836400	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr1:77826400-77831000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr1:77826400-77834200	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr1:77826800-77828800	Strong transcription	NHDF-Ad	bronchial
32	chr1:77826800-77834200	Weak transcription	HSMM	muscle
33	chr1:77828800-77829200	Genic enhancers	NHDF-Ad	bronchial
34	chr1:77829200-77834000	Weak transcription	NHDF-Ad	bronchial
35	chr1:77830200-77835200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr1:77831000-77831600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
37	chr1:77831200-77831600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr1:77831600-77835600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr1:77831600-77835800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr1:77833200-77835800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr1:77834000-77839800	Enhancers	NHDF-Ad	bronchial
42	chr1:77834200-77834400	Enhancers	Brain Cingulate Gyrus	brain
43	chr1:77834200-77834600	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr1:77834200-77834600	Enhancers	Brain Substantia Nigra	brain
45	chr1:77834200-77835600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr1:77834200-77835600	Enhancers	HSMM	muscle
47	chr1:77834200-77836400	Enhancers	Muscle Satellite Cultured Cells	--
48	chr1:77834200-77836600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr1:77834200-77839000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr1:77834400-77835200	Weak transcription	Brain Cingulate Gyrus	brain

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