Variant report

Variant	esv3355513
Chromosome Location	chr7:150670544-150673392
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:25)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:150661173..150665225-chr7:150669426..150673358,7	MCF-7	breast:
2	chr12:65259282..65261612-chr7:150671119..150672990,2	MCF-7	breast:
3	chr7:150627605..150628492-chr7:150671224..150672069,2	K562	blood:
4	chr7:150594719..150596784-chr7:150671045..150673400,2	MCF-7	breast:
5	chr7:150671324..150673603-chr7:150688182..150691343,3	MCF-7	breast:
6	chr7:150668944..150671861-chr7:150941507..150943455,2	MCF-7	breast:
7	chr7:150670508..150673387-chr7:150723224..150725668,3	MCF-7	breast:
8	chr7:150671828..150674694-chr7:150692153..150695076,2	MCF-7	breast:
9	chr7:150671455..150673565-chr7:150752052..150755338,3	MCF-7	breast:
10	chr11:592285..592822-chr7:150671646..150672236,2	MCF-7	breast:
11	chr7:150671778..150674151-chr7:150678272..150681379,4	MCF-7	breast:
12	chr7:150668903..150671561-chr7:150807024..150809833,2	MCF-7	breast:
13	chr7:150654976..150656696-chr7:150671274..150673215,2	MCF-7	breast:
14	chr7:150670110..150672033-chr7:150810426..150812934,2	MCF-7	breast:
15	chr7:150646673..150650094-chr7:150670937..150674779,4	MCF-7	breast:
16	chr7:150669264..150677850-chr7:150681612..150689209,13	MCF-7	breast:
17	chr7:150670653..150672364-chr7:150715220..150718108,2	MCF-7	breast:
18	chr19:55918635..55919319-chr7:150671393..150672297,2	HCT-116	colon:
19	chr7:150670321..150673113-chr7:150933266..150935781,2	MCF-7	breast:
20	chr7:150670317..150671058-chr7:150682793..150683490,2	K562	blood:
21	chr7:150671887..150673971-chr7:150915991..150917932,2	K562	blood:
22	chr7:150654869..150656816-chr7:150670691..150673405,2	MCF-7	breast:
23	chr7:150671805..150672600-chr7:150682853..150683837,2	K562	blood:
24	chr7:150634464..150636964-chr7:150670317..150672404,2	MCF-7	breast:
25	chr7:150661035..150665420-chr7:150665668..150673641,9	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000164889	chromatin interactions
ENSG00000164867	chromatin interactions
ENSG00000211517	chromatin interactions
ENSG00000082014	chromatin interactions
ENSG00000108106	chromatin interactions
ENSG00000197150	chromatin interactions
ENSG00000133612	chromatin interactions
ENSG00000164885	chromatin interactions
ENSG00000181652	chromatin interactions

Extended variants
information (count: 148 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:148 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55642626	chr7:150670727-150670728	Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs3778871	chr7:150670772-150670773	Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs559159865	chr7:150670811-150670812	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs528209388	chr7:150670871-150670872	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs35984356	chr7:150670919-150670920	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs116737870	chr7:150670943-150670944	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs564712451	chr7:150670951-150670952	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs149799564	chr7:150670952-150670953	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs541028405	chr7:150670965-150670966	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs552918620	chr7:150670977-150670978	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs3778870	chr7:150670992-150670993	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs542500166	chr7:150671066-150671067	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs3778869	chr7:150671098-150671099	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs535437292	chr7:150671125-150671126	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs183136504	chr7:150671181-150671182	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs3800779	chr7:150671214-150671215	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs145740426	chr7:150671245-150671246	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs41308996	chr7:150671276-150671277	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs564839791	chr7:150671277-150671278	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs41311033	chr7:150671296-150671297	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs377495794	chr7:150671299-150671300	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs557623251	chr7:150671388-150671389	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs560000582	chr7:150671426-150671427	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs748693	chr7:150671437-150671438	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs116568934	chr7:150671487-150671488	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs549331225	chr7:150671520-150671521	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs371695614	chr7:150671527-150671528	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs186151214	chr7:150671617-150671618	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs116065480	chr7:150671677-150671678	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs190913987	chr7:150671708-150671709	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs572808768	chr7:150671717-150671718	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs373703502	chr7:150671763-150671764	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs139968479	chr7:150671769-150671770	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs200121781	chr7:150671772-150671773	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs201872229	chr7:150671793-150671794	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs199472857	chr7:150671801-150671802	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs199472856	chr7:150671805-150671806	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs199472855	chr7:150671807-150671808	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs121912515	chr7:150671808-150671809	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs199472854	chr7:150671810-150671811	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs549995059	chr7:150671817-150671818	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs199472853	chr7:150671819-150671820	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs199473496	chr7:150671820-150671821	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs199472852	chr7:150671825-150671826	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs563611707	chr7:150671832-150671833	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs199473495	chr7:150671846-150671847	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
47	rs199472851	chr7:150671849-150671850	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
48	rs199473494	chr7:150671852-150671853	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs199472850	chr7:150671853-150671854	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
50	rs199472849	chr7:150671863-150671864	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:525 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150658200-150670800	Enhancers	Rectal Smooth Muscle	rectum
2	chr7:150664400-150673600	Enhancers	Fetal Lung	lung
3	chr7:150664600-150674000	Enhancers	Fetal Brain Male	brain
4	chr7:150665200-150671800	Genic enhancers	Fetal Stomach	stomach
5	chr7:150665400-150671800	Enhancers	Left Ventricle	heart
6	chr7:150665600-150671200	Enhancers	Right Ventricle	heart
7	chr7:150666200-150670800	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr7:150666400-150671400	Enhancers	Fetal Thymus	thymus
9	chr7:150666800-150671400	Enhancers	Fetal Intestine Large	intestine
10	chr7:150667200-150672400	Enhancers	Fetal Heart	heart
11	chr7:150667600-150670800	Flanking Active TSS	Stomach Smooth Muscle	stomach
12	chr7:150668000-150671200	Enhancers	Brain Anterior Caudate	brain
13	chr7:150668200-150671800	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr7:150668400-150670800	Enhancers	Placenta	Placenta
15	chr7:150668400-150671600	Enhancers	Right Atrium	heart
16	chr7:150668800-150671000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr7:150668800-150671200	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr7:150669000-150670600	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr7:150669000-150670800	Weak transcription	Gastric	stomach
20	chr7:150669000-150671200	Weak transcription	K562	blood
21	chr7:150669200-150670600	Weak transcription	Spleen	Spleen
22	chr7:150669200-150670800	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr7:150669200-150670800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr7:150669200-150671200	Enhancers	Brain Germinal Matrix	brain
25	chr7:150669200-150671800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
26	chr7:150669600-150670600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:150669600-150670800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr7:150669600-150670800	Enhancers	Brain Cingulate Gyrus	brain
29	chr7:150669600-150670800	Weak transcription	HSMM	muscle
30	chr7:150669600-150671000	Weak transcription	Esophagus	oesophagus
31	chr7:150669600-150671200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr7:150669600-150671200	Enhancers	Primary T cells fromperipheralblood	blood
33	chr7:150669600-150671200	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr7:150669600-150671400	Weak transcription	Brain Angular Gyrus	brain
35	chr7:150669600-150671800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:150669600-150671800	Weak transcription	Brain Hippocampus Middle	brain
37	chr7:150669600-150671800	Weak transcription	Small Intestine	intestine
38	chr7:150669800-150670600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr7:150669800-150670800	Weak transcription	Duodenum Mucosa	Duodenum
40	chr7:150669800-150671200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr7:150669800-150671200	Weak transcription	Fetal Brain Female	brain
42	chr7:150669800-150671200	Weak transcription	Ovary	ovary
43	chr7:150669800-150671800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr7:150669800-150671800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr7:150669800-150671800	Enhancers	Colon Smooth Muscle	Colon
46	chr7:150669800-150671800	Bivalent Enhancer	Fetal Muscle Leg	muscle
47	chr7:150670000-150670600	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr7:150670000-150671000	Weak transcription	Lung	lung
49	chr7:150670000-150671200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
50	chr7:150670000-150672400	Weak transcription	HSMMtube	muscle

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