Variant report

Variant	esv1848735
Chromosome Location	chr1:77885282-77918347
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	chr1:77902445-77902509	K562	blood:	n/a	n/a
2	CEBPB	chr1:77889964-77890298	IMR90	lung:	n/a	n/a
3	CEBPB	chr1:77898373-77898681	HepG2	liver:	n/a	chr1:77898501-77898512
4	CEBPB	chr1:77896726-77897014	IMR90	lung:	n/a	n/a
5	CEBPB	chr1:77898338-77898655	IMR90	lung:	n/a	chr1:77898501-77898512
6	CEBPB	chr1:77898345-77898693	Hela-S3	cervix:	n/a	chr1:77898501-77898512
7	CEBPB	chr1:77896771-77897011	A549	lung:	n/a	n/a
8	CEBPB	chr1:77898368-77898668	A549	lung:	n/a	chr1:77898501-77898512
9	CEBPB	chr1:77896833-77896892	K562	blood:	n/a	n/a
10	CEBPB	chr1:77897502-77897612	A549	lung:	n/a	n/a
11	CTCF	chr1:77914864-77914964	ProgFib	skin:	n/a	n/a
12	CTCF	chr1:77914840-77914990	GM12873	blood:	n/a	n/a
13	CTCF	chr1:77908400-77908550	HA-sp	spinal cord:	n/a	n/a
14	CTCF	chr1:77914800-77914950	K562	blood:	n/a	n/a
15	CTCF	chr1:77914780-77914930	HepG2	liver:	n/a	n/a
16	CTCF	chr1:77901246-77901271	Gliobla	brain:	n/a	n/a
17	CUX1	chr1:77885637-77885731	GM12878	blood:	n/a	n/a
18	E2F4	chr1:77903184-77903347	MCF10A-Er-Src	breast:	n/a	n/a
19	EGR1	chr1:77913447-77913769	MCF-7	breast:	n/a	n/a
20	EP300	chr1:77913243-77913869	A549	lung:	n/a	chr1:77913552-77913562 chr1:77913395-77913404
21	EP300	chr1:77901521-77901565	GM12878	blood:	n/a	n/a
22	FOS	chr1:77915444-77915459	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr1:77889910-77890324	MCF10A-Er-Src	breast:	n/a	chr1:77890128-77890139
24	FOS	chr1:77889963-77890373	MCF10A-Er-Src	breast:	n/a	chr1:77890128-77890139
25	FOS	chr1:77889963-77890377	MCF10A-Er-Src	breast:	n/a	chr1:77890128-77890139
26	FOS	chr1:77889959-77890322	MCF10A-Er-Src	breast:	n/a	chr1:77890128-77890139
27	FOS	chr1:77898347-77898651	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr1:77898436-77898636	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr1:77889902-77890490	HUVEC	blood vessel:	n/a	chr1:77890128-77890139
30	FOSL2	chr1:77889919-77890288	SK-N-SH	brain:	n/a	n/a
31	FOSL2	chr1:77913272-77913671	A549	lung:	n/a	n/a
32	FOSL2	chr1:77889878-77890400	SK-N-SH	brain:	n/a	n/a
33	FOXA1	chr1:77913250-77913647	T-47D	breast:	n/a	chr1:77913551-77913566 chr1:77913497-77913509 chr1:77913553-77913565
34	FOXA1	chr1:77913380-77913657	T-47D	breast:	n/a	chr1:77913551-77913566 chr1:77913497-77913509 chr1:77913553-77913565
35	FOXA1	chr1:77913331-77913666	HepG2	liver:	n/a	chr1:77913551-77913566 chr1:77913497-77913509 chr1:77913553-77913565
36	FOXA1	chr1:77913398-77913644	HepG2	liver:	n/a	chr1:77913551-77913566 chr1:77913497-77913509 chr1:77913553-77913565
37	FOXA2	chr1:77913357-77913822	A549	lung:	n/a	chr1:77913497-77913509 chr1:77913553-77913565
38	FOXA2	chr1:77913395-77913670	HepG2	liver:	n/a	chr1:77913497-77913509 chr1:77913553-77913565
39	FOXA2	chr1:77913269-77913851	A549	lung:	n/a	chr1:77913497-77913509 chr1:77913553-77913565
40	FOXM1	chr1:77903457-77904555	SK-N-SH	brain:	n/a	n/a
41	FOXM1	chr1:77903772-77904346	SK-N-SH	brain:	n/a	n/a
42	GATA3	chr1:77903902-77904530	MCF-7	breast:	n/a	n/a
43	GATA3	chr1:77899012-77899386	MCF-7	breast:	n/a	n/a
44	GATA3	chr1:77904962-77905662	SK-N-SH	brain:	n/a	n/a
45	GATA3	chr1:77913132-77913819	MCF-7	breast:	n/a	chr1:77913138-77913148
46	GATA3	chr1:77903756-77904682	SK-N-SH	brain:	n/a	n/a
47	GATA3	chr1:77899074-77899510	MCF-7	breast:	n/a	n/a
48	GATA3	chr1:77903833-77904602	SK-N-SH	brain:	n/a	n/a
49	GATA3	chr1:77913193-77913875	A549	lung:	n/a	n/a
50	GATA3	chr1:77913156-77913838	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:77912654-77912704	Hepatocyte	liver:	n/a
2	chr1:77912654-77912704	Hepatocyte	liver:	n/a
3	chr1:77904032-77904082	HRCEpiC	kidney:	n/a
4	chr1:77912654-77912704	AG09309	skin:	n/a
5	chr1:77904032-77904082	T-47D	breast:	n/a
6	chr1:77912654-77912704	HCM	heart:	n/a
7	chr1:77912654-77912704	HMEC	breast:	n/a
8	chr1:77904032-77904082	BE2_C	brain:	n/a
9	chr1:77904032-77904082	SK-N-SH_RA	brain:	n/a
10	chr1:77904032-77904082	HNPCEpiC	eye:	n/a
11	chr1:77904032-77904082	PFSK-1	brain:	n/a
12	chr1:77904032-77904082	RPTEC	kidney:	n/a
13	chr1:77904032-77904082	HL-60	blood:	n/a
14	chr1:77912654-77912704	HRPEpiC	eye:	n/a
15	chr1:77912654-77912704	T-47D	breast:	n/a
16	chr1:77904032-77904082	SK-N-MC	brain:	n/a
17	chr1:77904032-77904082	ProgFib	skin:	n/a
18	chr1:77904032-77904082	A549	lung:	n/a
19	chr1:77912654-77912704	SKMC	muscle:	n/a
20	chr1:77912654-77912704	GM12878	blood:	n/a
21	chr1:77912654-77912704	PANC-1	pancreas:	n/a
22	chr1:77904032-77904082	HPAEpiC	pulmonary alveolar:	n/a
23	chr1:77912654-77912704	U87	brain:	n/a
24	chr1:77912654-77912704	A549	lung:	n/a
25	chr1:77912654-77912704	BJ	skin:	n/a
26	chr1:77904032-77904082	SAEC	small airway:	n/a
27	chr1:77912654-77912704	SAEC	small airway:	n/a
28	chr1:77904032-77904082	GM12892	blood:	n/a
29	chr1:77912654-77912704	AG04450	lung:	fetal
30	chr1:77912654-77912704	HCF	heart:	n/a
31	chr1:77912654-77912704	GM12891	blood:	n/a
32	chr1:77912654-77912704	Hela-S3	cervix:	n/a
33	chr1:77912654-77912704	K562	blood:	n/a
34	chr1:77912654-77912704	GM12892	blood:	n/a
35	chr1:77912654-77912704	HUVEC	blood vessel:	n/a
36	chr1:77912654-77912704	NB4	blood:	n/a
37	chr1:77912654-77912704	GM06990	blood:	n/a
38	chr1:77904032-77904082	HCM	heart:	n/a
39	chr1:77904032-77904082	GM06990	blood:	n/a
40	chr1:77912654-77912704	SK-N-MC	brain:	n/a
41	chr1:77912654-77912704	NHBE	bronchial:	n/a
42	chr1:77904032-77904082	ECC-1	luminal epithelium:	n/a
43	chr1:77904032-77904082	HAEpiC	amniotic membrane:	n/a
44	chr1:77912654-77912704	HRE	kidney:	n/a
45	chr1:77912654-77912704	HAEpiC	amniotic membrane:	n/a
46	chr1:77904032-77904082	HEEpiC	esophagus:	n/a
47	chr1:77904032-77904082	HIPEpiC	eye:	n/a
48	chr1:77904032-77904082	AG09309	skin:	n/a
49	chr1:77904032-77904082	AG04449	skin:	fetal
50	chr1:77912654-77912704	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:77884906..77887618-chr1:77887940..77890792,2	K562	blood:
2	chr1:77915846..77918627-chr1:77942564..77944973,2	K562	blood:
3	chr1:77898654..77900844-chr1:77900858..77902632,2	K562	blood:
4	chr1:77898654..77900844-chr1:77900858..77902632,2	K562	blood:
5	chr1:77897440..77899362-chr1:78468491..78471340,2	K562	blood:

Variant related genes	Relation type
RNU7-8P	TF binding region
RNU7-8P	CpG island
ENSG00000273338	chromatin interactions
ENSG00000162616	chromatin interactions
ENSG00000251767	chromatin interactions

Extended variants
information (count: 1242 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1242 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9633478	chr1:77885282-77885283	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs74092615	chr1:77885307-77885308	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs9633479	chr1:77885315-77885316	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs533212803	chr1:77885330-77885331	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201078225	chr1:77885369-77885370	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145242679	chr1:77885371-77885372	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546264261	chr1:77885384-77885385	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs183479749	chr1:77885457-77885458	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531876155	chr1:77885462-77885463	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550275576	chr1:77885482-77885483	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs141691215	chr1:77885512-77885513	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs146363152	chr1:77885559-77885560	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547629354	chr1:77885580-77885581	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188368175	chr1:77885582-77885583	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs193195455	chr1:77885624-77885625	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557367183	chr1:77885641-77885642	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs9633480	chr1:77885657-77885658	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs185494791	chr1:77885693-77885694	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs555458282	chr1:77885710-77885711	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs573612111	chr1:77885711-77885712	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs541222314	chr1:77885777-77885778	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370126083	chr1:77885820-77885821	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543046760	chr1:77885828-77885829	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139725400	chr1:77885873-77885874	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs578028179	chr1:77885891-77885892	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545306571	chr1:77885899-77885900	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564499270	chr1:77885915-77885916	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531759497	chr1:77885935-77885936	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543417446	chr1:77886010-77886011	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552774299	chr1:77886026-77886027	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528783042	chr1:77886050-77886051	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573019903	chr1:77886083-77886084	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535290904	chr1:77886111-77886112	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187840660	chr1:77886118-77886119	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35282414	chr1:77886122-77886123	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs66532354	chr1:77886131-77886132	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs398089371	chr1:77886132-77886133	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34326091	chr1:77886227-77886228	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs3104461	chr1:77886339-77886340	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs548011230	chr1:77886416-77886417	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191142759	chr1:77886446-77886447	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544472920	chr1:77886456-77886457	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs202026482	chr1:77886458-77886459	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533475694	chr1:77886498-77886499	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs10493606	chr1:77886499-77886500	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs569982786	chr1:77886514-77886515	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536660768	chr1:77886559-77886560	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2647485	chr1:77886570-77886571	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs2351031	chr1:77886578-77886579	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373891457	chr1:77886617-77886618	Weak transcription Enhancers 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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77872200-77893400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr1:77872200-77913800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr1:77876600-77888600	Strong transcription	HSMM	muscle
4	chr1:77878000-77887000	Weak transcription	Brain Angular Gyrus	brain
5	chr1:77878600-77886400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr1:77878800-77886400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr1:77879200-77887200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr1:77879600-77887200	Weak transcription	Fetal Thymus	thymus
9	chr1:77879600-77887800	Weak transcription	Brain Substantia Nigra	brain
10	chr1:77879800-77885800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr1:77879800-77886600	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr1:77879800-77887200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr1:77879800-77887400	Weak transcription	Brain Hippocampus Middle	brain
14	chr1:77880000-77887200	Weak transcription	Brain Anterior Caudate	brain
15	chr1:77880200-77886200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr1:77880400-77886200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr1:77882600-77889000	Weak transcription	NHLF	lung
18	chr1:77883000-77886200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr1:77883000-77889800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr1:77883400-77888600	Strong transcription	Muscle Satellite Cultured Cells	--
21	chr1:77884000-77889400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr1:77884200-77885400	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr1:77884200-77885600	Weak transcription	Primary T cells from cord blood	blood
24	chr1:77884200-77885600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr1:77884200-77887000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr1:77884200-77887200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr1:77884400-77885400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr1:77884400-77886800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr1:77884400-77890400	Enhancers	Primary T helper cells fromperipheralblood	blood
30	chr1:77884600-77887200	Weak transcription	Primary hematopoietic stem cells	blood
31	chr1:77884600-77889600	Weak transcription	Osteobl	bone
32	chr1:77884800-77889400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
33	chr1:77884800-77890600	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr1:77885000-77886200	Weak transcription	NHDF-Ad	bronchial
35	chr1:77885000-77886800	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr1:77885000-77887200	Weak transcription	HSMMtube	muscle
37	chr1:77885200-77885400	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr1:77885200-77886600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr1:77885200-77887000	Weak transcription	Brain Cingulate Gyrus	brain
40	chr1:77885400-77886800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr1:77885400-77890600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr1:77885600-77887000	Enhancers	Primary T cells from cord blood	blood
43	chr1:77885600-77887200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr1:77885600-77888400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
45	chr1:77885600-77888400	Enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr1:77885800-77886000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr1:77885800-77888200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
48	chr1:77886000-77886400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr1:77886200-77886600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr1:77886200-77887200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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