Variant report

Variant	esv3428582
Chromosome Location	chr7:141013551-141064197
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:360)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:360 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:141042310-141042316	K562	blood:	n/a	n/a
2	BACH1	chr7:141062874-141063098	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr7:141016902-141017172	GM12878	blood:	n/a	n/a
4	BATF	chr7:141016927-141017222	GM12878	blood:	n/a	n/a
5	CEBPB	chr7:141029186-141029384	HepG2	liver:	n/a	chr7:141029340-141029351
6	CEBPB	chr7:141033180-141033543	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr7:141024456-141024802	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr7:141059089-141059233	H1-hESC	embryonic stem cell:	n/a	chr7:141059113-141059126 chr7:141059113-141059126 chr7:141059115-141059126
9	CEBPB	chr7:141062445-141062550	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPZ	chr7:141033156-141033225	HepG2	liver:	n/a	n/a
11	CTCF	chr7:141042560-141042710	HRE	kidney:	n/a	n/a
12	CTCF	chr7:141051740-141051890	GM12869	blood:	n/a	n/a
13	CTCF	chr7:141035042-141035223	K562	blood:	n/a	n/a
14	CTCF	chr7:141051980-141052130	GM12869	blood:	n/a	n/a
15	CTCF	chr7:141052040-141052190	GM12878	blood:	n/a	chr7:141052119-141052137
16	CTCF	chr7:141036841-141037134	GM19239	blood:	n/a	n/a
17	CTCF	chr7:141051960-141052110	GM12872	blood:	n/a	n/a
18	CTCF	chr7:141052020-141052170	HCFaa	heart:	n/a	chr7:141052119-141052137
19	CTCF	chr7:141052020-141052170	HepG2	liver:	n/a	chr7:141052119-141052137
20	CTCF	chr7:141040402-141040424	LNCaP	prostate:	n/a	n/a
21	CTCF	chr7:141028108-141028344	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr7:141052000-141052150	K562	blood:	n/a	chr7:141052119-141052137
23	CTCF	chr7:141051900-141052050	GM12864	blood:	n/a	n/a
24	CTCF	chr7:141062648-141062698	ProgFib	skin:	n/a	n/a
25	CTCF	chr7:141027580-141027730	NHLF	lung:	n/a	n/a
26	CTCF	chr7:141052020-141052170	HBMEC	blood vessel:	n/a	chr7:141052119-141052137
27	CTCF	chr7:141035120-141035270	MCF-7	breast:	n/a	n/a
28	CTCF	chr7:141051980-141052130	HEK293	kidney:	n/a	n/a
29	CTCF	chr7:141055867-141055956	Lung_OC	lung:	n/a	n/a
30	CTCF	chr7:141035060-141035210	HCT-116	colon:	n/a	n/a
31	CTCF	chr7:141035058-141035194	K562	blood:	n/a	n/a
32	CTCF	chr7:141014649-141014677	GM13976	blood:	n/a	n/a
33	CTCF	chr7:141055120-141055270	RPTEC	kidney:	n/a	n/a
34	CTCF	chr7:141055040-141055190	HMF	breast:	n/a	n/a
35	CTCF	chr7:141035097-141035265	A549	lung:	n/a	n/a
36	CTCF	chr7:141028225-141028244	GM12878	blood:	n/a	n/a
37	CTCF	chr7:141036614-141036729	GM19239	blood:	n/a	n/a
38	CTCF	chr7:141052000-141052150	GM12873	blood:	n/a	chr7:141052119-141052137
39	CTCF	chr7:141035120-141035270	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr7:141035088-141035249	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr7:141040369-141040469	K562	blood:	n/a	chr7:141040395-141040416 chr7:141040400-141040418
42	CTCF	chr7:141052020-141052170	HUVEC	blood vessel:	n/a	chr7:141052119-141052137
43	CTCF	chr7:141052040-141052190	MCF-7	breast:	n/a	chr7:141052119-141052137
44	CTCF	chr7:141035080-141035230	GM12873	blood:	n/a	n/a
45	CTCF	chr7:141033384-141033455	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr7:141052000-141052150	GM12874	blood:	n/a	chr7:141052119-141052137
47	CTCF	chr7:141055080-141055230	HMF	breast:	n/a	n/a
48	CTCF	chr7:141028040-141028190	HMEC	breast:	n/a	n/a
49	CTCF	chr7:141028140-141028290	HMEC	breast:	n/a	n/a
50	CTCF	chr7:141028100-141028250	HMF	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:141024673-141024723	HCF	heart:	n/a
2	chr7:141024673-141024723	GM12891	blood:	n/a
3	chr7:141024673-141024723	HL-60	blood:	n/a
4	chr7:141024673-141024723	GM06990	blood:	n/a
5	chr7:141024673-141024723	PrEC	prostate:	n/a
6	chr7:141024673-141024723	AG09309	skin:	n/a
7	chr7:141024673-141024723	NHBE	bronchial:	n/a
8	chr7:141024673-141024723	Hepatocyte	liver:	n/a
9	chr7:141024673-141024723	AG10803	skin:	n/a
10	chr7:141024673-141024723	CMK	blood:	n/a
11	chr7:141024673-141024723	ProgFib	skin:	n/a
12	chr7:141024673-141024723	HNPCEpiC	eye:	n/a
13	chr7:141024673-141024723	SKMC	muscle:	n/a
14	chr7:141024673-141024723	NH-A	brain:	n/a
15	chr7:141024673-141024723	HUVEC	blood vessel:	n/a
16	chr7:141024673-141024723	SK-N-MC	brain:	n/a
17	chr7:141024673-141024723	A549	lung:	n/a
18	chr7:141024673-141024723	AG04450	lung:	fetal
19	chr7:141024673-141024723	IMR90	lung:	fetal
20	chr7:141024673-141024723	HEEpiC	esophagus:	n/a
21	chr7:141024673-141024723	PFSK-1	brain:	n/a
22	chr7:141024673-141024723	HRCEpiC	kidney:	n/a
23	chr7:141024673-141024723	SAEC	small airway:	n/a
24	chr7:141024673-141024723	HepG2	liver:	n/a
25	chr7:141024673-141024723	GM12878	blood:	n/a
26	chr7:141024673-141024723	HEK293	kidney:	embryo
27	chr7:141024673-141024723	AG04449	skin:	fetal
28	chr7:141024673-141024723	HCM	heart:	n/a
29	chr7:141024673-141024723	SK-N-SH	brain:	n/a
30	chr7:141024673-141024723	T-47D	breast:	n/a
31	chr7:141024673-141024723	NB4	blood:	n/a
32	chr7:141024673-141024723	BE2_C	brain:	n/a
33	chr7:141024673-141024723	ECC-1	luminal epithelium:	n/a
34	chr7:141024673-141024723	NT2-D1	testis:	n/a
35	chr7:141024673-141024723	RPTEC	kidney:	n/a
36	chr7:141024673-141024723	HRPEpiC	eye:	n/a
37	chr7:141024673-141024723	MCF10A-Er-Src	breast:	n/a
38	chr7:141024673-141024723	SK-N-SH_RA	brain:	n/a
39	chr7:141024673-141024723	HCT-116	colon:	n/a
40	chr7:141024673-141024723	MCF-7	breast:	n/a
41	chr7:141024673-141024723	HPAEpiC	pulmonary alveolar:	n/a
42	chr7:141024673-141024723	BJ	skin:	n/a
43	chr7:141024673-141024723	ovcar-3	ovarian:	n/a
44	chr7:141024673-141024723	AoSMC	blood vessel:	n/a
45	chr7:141024673-141024723	Jurkat	blood:	n/a
46	chr7:141024673-141024723	K562	blood:	n/a
47	chr7:141024673-141024723	Caco-2	colon:	n/a
48	chr7:141024673-141024723	HAEpiC	amniotic membrane:	n/a
49	chr7:141024673-141024723	U87	brain:	n/a
50	chr7:141024673-141024723	GM19239	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:141034745..141035250-chr7:141232846..141233551,2	MCF-7	breast:
2	chr7:141029015..141031882-chr7:141078726..141080854,2	K562	blood:
3	chr7:141026635..141028691-chr7:141030665..141032279,2	K562	blood:
4	chr7:141010882..141013752-chr7:141015205..141017324,2	K562	blood:
5	chr7:141010882..141013752-chr7:141015205..141017324,2	K562	blood:
6	chr7:141056651..141059376-chr7:141061286..141063035,2	K562	blood:
7	chr7:141056651..141059376-chr7:141061286..141063035,2	K562	blood:
8	chr7:141026635..141028691-chr7:141030665..141032279,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA1147-6	chr7:141050607-141052026	refGeneNc_2015_NR_015392
2	lnc-AGK-4	chr7:141051777-141052163	NONHSAT123709
3	lnc-AGK-4	chr7:141052478-141052568	NONHSAT123709
4	lnc-KIAA1147-6	chr7:141060458-141060643	refGeneNc_2015_NR_015392

No data

Variant related genes	Relation type
ENSG00000261624	TF binding region
ENSG00000261624	CpG island

Extended variants
information (count: 1870 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1870 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147370932	chr7:141013555-141013556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs567339984	chr7:141013613-141013614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs374857279	chr7:141013617-141013618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs538539279	chr7:141013682-141013683	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528250730	chr7:141013720-141013721	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571531102	chr7:141013743-141013744	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs538968133	chr7:141013750-141013751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs556973332	chr7:141013765-141013766	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374775078	chr7:141013769-141013770	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs568915994	chr7:141013852-141013853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs139586183	chr7:141013868-141013869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs188898186	chr7:141013875-141013876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs572852156	chr7:141013897-141013898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs200252899	chr7:141013913-141013914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs540794450	chr7:141013952-141013953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs115428396	chr7:141013996-141013997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs367796024	chr7:141014033-141014034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs143612041	chr7:141014094-141014095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs544534939	chr7:141014183-141014184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs193115570	chr7:141014192-141014193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs184334803	chr7:141014202-141014203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114619186	chr7:141014257-141014258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560588087	chr7:141014266-141014267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs569763165	chr7:141014303-141014304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs375042566	chr7:141014306-141014307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189280048	chr7:141014323-141014324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs546801081	chr7:141014333-141014334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs565103797	chr7:141014355-141014356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs144079393	chr7:141014387-141014388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs116534246	chr7:141014398-141014399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs12539111	chr7:141014400-141014401	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs112380125	chr7:141014422-141014423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs377640938	chr7:141014441-141014442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191724320	chr7:141014523-141014524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs200604744	chr7:141014533-141014534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs533687710	chr7:141014557-141014558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs148689166	chr7:141014711-141014712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs142193048	chr7:141014730-141014731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538140244	chr7:141014748-141014749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184316609	chr7:141014763-141014764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs151224073	chr7:141014824-141014825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs542170668	chr7:141014854-141014855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs560319388	chr7:141014857-141014858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs572480066	chr7:141014861-141014862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs139476582	chr7:141014887-141014888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs373016609	chr7:141014894-141014895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565062053	chr7:141014919-141014920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs376544385	chr7:141014920-141014921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs189051077	chr7:141014937-141014938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs144215476	chr7:141014982-141014983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell acute lymphoblastic leukemia	16673021	CNVD
Cancer	21183584	CNVD
Intracranial ependymoma	16609018	CNVD
Non-small cell lung cancer	21829676	CNVD
Developmental delay	19490664	CNVD
Pancreatitis	20877625	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16968546	CNVD
Pilocytic astrocytoma	18408760	CNVD
Idiopathic chronic pancreatitis	19584086	CNVD
Low-grade astrocytoma	19016743	CNVD
Pediatric low-grade astrocytoma	19016743	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Gastric cancer	16891809	CNVD
Cancer	17440070	CNVD
Astrocytoma	18398503	CNVD
Melanoma	19671679	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
Glioblastoma multiforme	21525872	CNVD
Breast cancer	21509527	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:453 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:140994400-141018000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr7:141004600-141014200	Weak transcription	Right Atrium	heart
3	chr7:141012400-141013800	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr7:141013000-141013800	Enhancers	Right Ventricle	heart
5	chr7:141013000-141016000	Enhancers	Left Ventricle	heart
6	chr7:141013200-141013600	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr7:141013400-141017000	Weak transcription	Psoas Muscle	Psoas
8	chr7:141013400-141019800	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr7:141013800-141014200	Weak transcription	Right Ventricle	heart
10	chr7:141013800-141016800	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr7:141014000-141014200	Enhancers	Fetal Brain Male	brain
12	chr7:141014200-141014400	Enhancers	Right Ventricle	heart
13	chr7:141014200-141014600	Enhancers	Right Atrium	heart
14	chr7:141014200-141018000	Weak transcription	Fetal Brain Male	brain
15	chr7:141014400-141029000	Weak transcription	Right Ventricle	heart
16	chr7:141014600-141025200	Weak transcription	Right Atrium	heart
17	chr7:141015600-141015800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr7:141015800-141016000	Enhancers	Fetal Brain Female	brain
19	chr7:141015800-141016800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr7:141016000-141018400	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr7:141016000-141024800	Weak transcription	Fetal Brain Female	brain
22	chr7:141016600-141016800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr7:141016800-141017400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr7:141016800-141017600	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr7:141016800-141025200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr7:141017000-141017400	Enhancers	Psoas Muscle	Psoas
27	chr7:141017600-141024800	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr7:141018000-141018200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
29	chr7:141018000-141019200	Enhancers	Fetal Brain Male	brain
30	chr7:141018200-141019000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr7:141019000-141019200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr7:141019200-141024400	Weak transcription	Fetal Brain Male	brain
33	chr7:141019800-141020400	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr7:141020000-141020400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr7:141020200-141020400	Enhancers	Left Ventricle	heart
36	chr7:141020400-141025000	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr7:141020400-141028200	Weak transcription	Left Ventricle	heart
38	chr7:141020600-141023800	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr7:141022200-141022600	Enhancers	Liver	Liver
40	chr7:141022400-141022600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr7:141022400-141022600	Enhancers	Brain Germinal Matrix	brain
42	chr7:141022600-141022800	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr7:141022600-141024600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr7:141022600-141024600	Weak transcription	Brain Germinal Matrix	brain
45	chr7:141022800-141023000	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr7:141022800-141024400	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr7:141023000-141024000	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr7:141023800-141024000	Enhancers	H1 Cell Line	embryonic stem cell
49	chr7:141024000-141024400	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr7:141024000-141025200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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