Variant report

Variant	esv3382945
Chromosome Location	chr1:77996914-77999212
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	CTCF	chr1:77999079-78000174	SK-N-SH	brain:	n/a	chr1:77999552-77999573 chr1:77999558-77999574 chr1:77999557-77999575
2	CTCF	chr1:77999209-78000262	A549	lung:	n/a	chr1:77999552-77999573 chr1:77999558-77999574 chr1:77999557-77999575
3	CTCF	chr1:77998720-77998870	GM12872	blood:	n/a	n/a
4	CTCF	chr1:77999159-78000007	IMR90	lung:	n/a	chr1:77999552-77999573 chr1:77999558-77999574 chr1:77999557-77999575
5	CTCF	chr1:77999180-77999330	GM12871	blood:	n/a	n/a
6	NFYA	chr1:77996841-77997190	K562	blood:	n/a	n/a
7	NFYB	chr1:77996951-77997146	Hela-S3	cervix:	n/a	chr1:77997047-77997062
8	NFYB	chr1:77996841-77997422	K562	blood:	n/a	chr1:77997047-77997062
9	NFYB	chr1:77996944-77997314	GM12878	blood:	n/a	chr1:77997047-77997062
10	POLR2A	chr1:77998389-77998392	ProgFib	skin:	n/a	n/a
11	POLR2A	chr1:77997485-77997950	PFSK-1	brain:	n/a	n/a
12	RAD21	chr1:77999123-78000083	SK-N-SH	brain:	n/a	chr1:77999555-77999574 chr1:77999345-77999357
13	RAD21	chr1:77999208-77999873	HCT-116	colon:	n/a	chr1:77999555-77999574 chr1:77999345-77999357
14	RAD21	chr1:77999191-78000104	A549	lung:	n/a	chr1:77999555-77999574 chr1:77999345-77999357
15	RXRA	chr1:77999138-77999846	SK-N-SH	brain:	n/a	chr1:77999555-77999575 chr1:77999560-77999567
16	SMC3	chr1:77999065-78000105	SK-N-SH	brain:	n/a	chr1:77999559-77999573
17	TCF12	chr1:77999209-77999999	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:77997502-77997552	HMEC	breast:	n/a
2	chr1:77997502-77997552	T-47D	breast:	n/a
3	chr1:77997502-77997552	BE2_C	brain:	n/a
4	chr1:77997502-77997552	Caco-2	colon:	n/a
5	chr1:77997502-77997552	K562	blood:	n/a
6	chr1:77997502-77997552	NHBE	bronchial:	n/a
7	chr1:77997502-77997552	GM06990	blood:	n/a
8	chr1:77997502-77997552	ovcar-3	ovarian:	n/a
9	chr1:77997502-77997552	U87	brain:	n/a
10	chr1:77997502-77997552	ECC-1	luminal epithelium:	n/a
11	chr1:77997502-77997552	HRE	kidney:	n/a
12	chr1:77997502-77997552	PrEC	prostate:	n/a
13	chr1:77997502-77997552	IMR90	lung:	fetal
14	chr1:77997502-77997552	SK-N-MC	brain:	n/a
15	chr1:77997502-77997552	RPTEC	kidney:	n/a
16	chr1:77997502-77997552	GM19239	blood:	n/a
17	chr1:77997502-77997552	AoSMC	blood vessel:	n/a
18	chr1:77997502-77997552	HEK293	kidney:	embryo
19	chr1:77997502-77997552	ProgFib	skin:	n/a
20	chr1:77997502-77997552	CMK	blood:	n/a
21	chr1:77997502-77997552	AG10803	skin:	n/a
22	chr1:77997502-77997552	LNCaP	prostate:	n/a
23	chr1:77997502-77997552	HCT-116	colon:	n/a
24	chr1:77997502-77997552	HNPCEpiC	eye:	n/a
25	chr1:77997502-77997552	HRCEpiC	kidney:	n/a
26	chr1:77997502-77997552	Hela-S3	cervix:	n/a
27	chr1:77997502-77997552	H1-hESC	embryonic stem cell:	embryo
28	chr1:77997502-77997552	SKMC	muscle:	n/a
29	chr1:77997502-77997552	A549	lung:	n/a
30	chr1:77997502-77997552	PFSK-1	brain:	n/a
31	chr1:77997502-77997552	AG09309	skin:	n/a
32	chr1:77997502-77997552	GM12878	blood:	n/a
33	chr1:77997502-77997552	NB4	blood:	n/a
34	chr1:77997502-77997552	HEEpiC	esophagus:	n/a
35	chr1:77997502-77997552	GM12891	blood:	n/a
36	chr1:77997502-77997552	HIPEpiC	eye:	n/a
37	chr1:77997502-77997552	MCF10A-Er-Src	breast:	n/a
38	chr1:77997502-77997552	BJ	skin:	n/a
39	chr1:77997502-77997552	NHDF-neo	bronchial:	n/a
40	chr1:77997502-77997552	GM12892	blood:	n/a
41	chr1:77997502-77997552	Jurkat	blood:	n/a
42	chr1:77997502-77997552	AG09319	gingival:	n/a
43	chr1:77997502-77997552	SK-N-SH_RA	brain:	n/a
44	chr1:77997502-77997552	AG04450	lung:	fetal
45	chr1:77997502-77997552	HL-60	blood:	n/a
46	chr1:77997502-77997552	HPAEpiC	pulmonary alveolar:	n/a
47	chr1:77997502-77997552	HCM	heart:	n/a
48	chr1:77997502-77997552	Hepatocyte	liver:	n/a
49	chr1:77997502-77997552	HAEpiC	amniotic membrane:	n/a
50	chr1:77997502-77997552	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:77996828..77998774-chr1:78147470..78149282,2	K562	blood:
2	chr1:76619553..76620451-chr1:77999109..77999974,2	K562	blood:

Variant related genes	Relation type
AK5	TF binding region
AK5	CpG island
ENSG00000036549	chromatin interactions

Extended variants
information (count: 106 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:106 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528436615	chr1:77996936-77996937	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs558613374	chr1:77996955-77996956	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs548497932	chr1:77996956-77996957	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs376804388	chr1:77996992-77996993	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs148549378	chr1:77996993-77996994	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs142921929	chr1:77997005-77997006	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs369269312	chr1:77997013-77997014	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs568312562	chr1:77997027-77997028	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs190395287	chr1:77997083-77997084	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs535900949	chr1:77997104-77997105	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs182585192	chr1:77997105-77997106	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs372305860	chr1:77997108-77997109	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs377131503	chr1:77997120-77997121	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs572432234	chr1:77997191-77997192	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs150677818	chr1:77997210-77997211	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs140174102	chr1:77997227-77997228	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs28890262	chr1:77997245-77997246	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs576593399	chr1:77997262-77997263	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs543639104	chr1:77997268-77997269	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs185272523	chr1:77997296-77997297	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs562452292	chr1:77997300-77997301	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs529533146	chr1:77997326-77997327	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs561087182	chr1:77997363-77997364	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs541285872	chr1:77997423-77997424	Strong transcription Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs558925926	chr1:77997444-77997445	Strong transcription Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs532736850	chr1:77997478-77997479	Strong transcription Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs189988333	chr1:77997517-77997518	Strong transcription Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs569632308	chr1:77997518-77997519	Strong transcription Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs530758801	chr1:77997519-77997520	Strong transcription Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs575173469	chr1:77997540-77997541	Strong transcription Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs534928047	chr1:77997541-77997542	Strong transcription Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs553259121	chr1:77997546-77997547	Strong transcription Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs562538942	chr1:77997560-77997561	Strong transcription Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs566103430	chr1:77997563-77997564	Strong transcription Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs2803171	chr1:77997590-77997591	Strong transcription Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs558266061	chr1:77997623-77997624	Strong transcription Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs143930681	chr1:77997659-77997660	Strong transcription Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
38	rs371302382	chr1:77997674-77997675	Strong transcription Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs373954560	chr1:77997675-77997676	Strong transcription Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs544035432	chr1:77997678-77997679	Strong transcription Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs555690626	chr1:77997688-77997689	Strong transcription Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs111552557	chr1:77997690-77997691	Strong transcription Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs78163096	chr1:77997693-77997694	Strong transcription Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs541346427	chr1:77997699-77997700	Strong transcription Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs12022986	chr1:77997740-77997741	Strong transcription Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs368904893	chr1:77997757-77997758	Strong transcription Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs2803170	chr1:77997768-77997769	Strong transcription Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs185786134	chr1:77997769-77997770	Strong transcription Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs530514268	chr1:77997770-77997771	Strong transcription Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs12731983	chr1:77997783-77997784	Strong transcription Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:108)

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
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:83 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77980800-77999400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr1:77981800-77998400	Weak transcription	Osteobl	bone
3	chr1:77981800-77999200	Weak transcription	NHLF	lung
4	chr1:77981800-77999400	Weak transcription	HSMMtube	muscle
5	chr1:77982000-77998200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:77982000-77998200	Weak transcription	Brain Angular Gyrus	brain
7	chr1:77982200-77998200	Weak transcription	Brain Anterior Caudate	brain
8	chr1:77983000-78009200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr1:77985200-77999400	Weak transcription	Brain Substantia Nigra	brain
10	chr1:77985400-77999800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr1:77988400-77999800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr1:77988600-77999400	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr1:77989000-77998200	Weak transcription	Brain Cingulate Gyrus	brain
14	chr1:77990400-77998200	Weak transcription	Brain Hippocampus Middle	brain
15	chr1:77992000-77998400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr1:77992000-77999000	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr1:77992000-77999200	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr1:77992000-77999200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr1:77992000-77999200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr1:77992200-77999200	Weak transcription	Primary T cells from cord blood	blood
21	chr1:77992200-77999200	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr1:77993400-77999400	Weak transcription	HSMM	muscle
23	chr1:77994400-77997800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr1:77995600-77998000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr1:77996400-77998200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr1:77996400-77998200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr1:77996400-77998200	Weak transcription	NHDF-Ad	bronchial
28	chr1:77996600-77997200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr1:77996600-77999600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr1:77996600-77999600	Weak transcription	HMEC	breast
31	chr1:77996800-77998200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr1:77996800-77998200	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr1:77996800-77999800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr1:77996800-77999800	Weak transcription	NHEK	skin
35	chr1:77996800-78001800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr1:77997200-77998000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr1:77997400-77997800	Active TSS	Placenta	Placenta
38	chr1:77997800-77998000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr1:77997800-77998000	Flanking Active TSS	Placenta	Placenta
40	chr1:77998000-77998600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr1:77998000-77998600	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr1:77998000-77998600	Enhancers	Placenta	Placenta
43	chr1:77998000-78014000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr1:77998200-77998600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr1:77998200-77998600	Enhancers	Brain Cingulate Gyrus	brain
46	chr1:77998200-77999400	Enhancers	Brain Anterior Caudate	brain
47	chr1:77998200-78000000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr1:77998200-78000000	Enhancers	NHDF-Ad	bronchial
49	chr1:77998200-78000200	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr1:77998200-78000200	Enhancers	Brain Angular Gyrus	brain

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