Variant report

Variant	nsv607663
Chromosome Location	chr7:78981719-79030922
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	CEBPB	chr7:79027775-79028070	A549	lung:	n/a	chr7:79028020-79028031
2	CEBPB	chr7:79011671-79012271	IMR90	lung:	n/a	chr7:79012088-79012097 chr7:79012088-79012097 chr7:79011726-79011739 chr7:79012087-79012098 chr7:79012088-79012097 chr7:79012086-79012099 chr7:79012086-79012097 chr7:79012085-79012102 chr7:79012088-79012097
3	CEBPB	chr7:79027875-79027924	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr7:79011964-79012277	A549	lung:	n/a	chr7:79012088-79012097 chr7:79012088-79012097 chr7:79012087-79012098 chr7:79012088-79012097 chr7:79012086-79012099 chr7:79012086-79012097 chr7:79012085-79012102 chr7:79012088-79012097
5	CEBPB	chr7:79006530-79006810	IMR90	lung:	n/a	n/a
6	CEBPB	chr7:79016623-79016661	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr7:79011980-79012224	K562	blood:	n/a	chr7:79012088-79012097 chr7:79012088-79012097 chr7:79012087-79012098 chr7:79012088-79012097 chr7:79012086-79012099 chr7:79012086-79012097 chr7:79012085-79012102 chr7:79012088-79012097
8	CEBPB	chr7:78987640-78987826	HepG2	liver:	n/a	n/a
9	CEBPB	chr7:79005323-79005646	HepG2	liver:	n/a	n/a
10	CEBPB	chr7:79027717-79028079	HepG2	liver:	n/a	chr7:79028020-79028031
11	CEBPB	chr7:79011670-79012272	HepG2	liver:	n/a	chr7:79012088-79012097 chr7:79012088-79012097 chr7:79011726-79011739 chr7:79012087-79012098 chr7:79012088-79012097 chr7:79012086-79012099 chr7:79012086-79012097 chr7:79012085-79012102 chr7:79012088-79012097
12	CTCF	chr7:78990620-78990770	GM12864	blood:	n/a	n/a
13	CTCF	chr7:78990560-78990710	GM12864	blood:	n/a	n/a
14	CTCF	chr7:78986920-78987070	HRPEpiC	eye:	n/a	n/a
15	CTCF	chr7:78986840-78986990	MCF-7	breast:	n/a	n/a
16	CTCF	chr7:78990620-78990770	HEEpiC	esophagus:	n/a	n/a
17	CTCF	chr7:78990640-78990790	Caco-2	colon:	n/a	n/a
18	CTCF	chr7:78990600-78990750	NHEK	skin:	n/a	n/a
19	CTCF	chr7:78990640-78990790	NHEK	skin:	n/a	n/a
20	CTCF	chr7:78990653-78990796	GM12892	blood:	n/a	n/a
21	CTCF	chr7:78990660-78990810	GM12867	blood:	n/a	n/a
22	CTCF	chr7:78990651-78990812	GM19239	blood:	n/a	n/a
23	CTCF	chr7:78990639-78990810	GM19238	blood:	n/a	n/a
24	CTCF	chr7:78990682-78990795	HepG2	liver:	n/a	n/a
25	CTCF	chr7:78990620-78990770	SAEC	small airway:	n/a	n/a
26	CTCF	chr7:78990620-78990770	GM12872	blood:	n/a	n/a
27	CTCF	chr7:78990640-78990790	HMEC	breast:	n/a	n/a
28	CTCF	chr7:78990675-78990762	LNCaP	prostate:	n/a	n/a
29	CTCF	chr7:78990640-78990790	GM12872	blood:	n/a	n/a
30	CTCF	chr7:78990720-78990870	GM12878	blood:	n/a	n/a
31	CTCF	chr7:78990420-78990570	A549	lung:	n/a	n/a
32	CTCF	chr7:78990700-78990850	BE2_C	brain:	n/a	n/a
33	CTCF	chr7:78990660-78990810	GM12870	blood:	n/a	n/a
34	CTCF	chr7:78990640-78990790	SAEC	small airway:	n/a	n/a
35	CTCF	chr7:78990620-78990770	GM12868	blood:	n/a	n/a
36	CTCF	chr7:78990632-78990780	HepG2	liver:	n/a	n/a
37	CTCF	chr7:78990659-78990797	GM12878	blood:	n/a	n/a
38	CTCF	chr7:78986840-78986990	RPTEC	kidney:	n/a	n/a
39	CTCF	chr7:78990640-78990790	GM12875	blood:	n/a	n/a
40	CTCF	chr7:78986880-78987030	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr7:78986900-78987050	Caco-2	colon:	n/a	n/a
42	CTCF	chr7:78990664-78990757	GM13977	blood:	n/a	n/a
43	CTCF	chr7:78990620-78990770	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr7:78986931-78987019	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr7:78990720-78990870	BJ	skin:	n/a	n/a
46	CTCF	chr7:78990660-78990811	LNCaP	prostate:	n/a	n/a
47	CTCF	chr7:78990680-78990830	HepG2	liver:	n/a	n/a
48	CTCF	chr7:78990620-78990770	GM06990	blood:	n/a	n/a
49	CTCF	chr7:78990660-78990810	GM12873	blood:	n/a	n/a
50	CTCF	chr7:78990612-78990847	NHEK	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:78982418-78982468	LNCaP	prostate:	n/a
2	chr7:78982418-78982468	Hepatocyte	liver:	n/a
3	chr7:78982418-78982468	HUVEC	blood vessel:	n/a
4	chr7:78982418-78982468	AG09309	skin:	n/a
5	chr7:78982418-78982468	AG04449	skin:	fetal
6	chr7:78982418-78982468	GM06990	blood:	n/a
7	chr7:78982418-78982468	Caco-2	colon:	n/a
8	chr7:78982418-78982468	HCPEpiC	choroid plexus:	n/a
9	chr7:78982418-78982468	MCF10A-Er-Src	breast:	n/a
10	chr7:78982418-78982468	ECC-1	luminal epithelium:	n/a
11	chr7:78982418-78982468	IMR90	lung:	fetal
12	chr7:78982418-78982468	SK-N-MC	brain:	n/a
13	chr7:78982418-78982468	HPAEpiC	pulmonary alveolar:	n/a
14	chr7:78982418-78982468	Jurkat	blood:	n/a
15	chr7:78982418-78982468	ovcar-3	ovarian:	n/a
16	chr7:78982418-78982468	GM12878	blood:	n/a
17	chr7:78982418-78982468	Hela-S3	cervix:	n/a
18	chr7:78982418-78982468	NB4	blood:	n/a
19	chr7:78982418-78982468	HRE	kidney:	n/a
20	chr7:78982418-78982468	T-47D	breast:	n/a
21	chr7:78982418-78982468	HIPEpiC	eye:	n/a
22	chr7:78982418-78982468	HCF	heart:	n/a
23	chr7:78982418-78982468	NHBE	bronchial:	n/a
24	chr7:78982418-78982468	U87	brain:	n/a
25	chr7:78982418-78982468	AG09319	gingival:	n/a
26	chr7:78982418-78982468	HEK293	kidney:	embryo
27	chr7:78982418-78982468	SKMC	muscle:	n/a
28	chr7:78982418-78982468	CMK	blood:	n/a
29	chr7:78982418-78982468	GM12892	blood:	n/a
30	chr7:78982418-78982468	HAEpiC	amniotic membrane:	n/a
31	chr7:78982418-78982468	HepG2	liver:	n/a
32	chr7:78982418-78982468	RPTEC	kidney:	n/a
33	chr7:78982418-78982468	PFSK-1	brain:	n/a
34	chr7:78982418-78982468	K562	blood:	n/a
35	chr7:78982418-78982468	HCT-116	colon:	n/a
36	chr7:78982418-78982468	HRCEpiC	kidney:	n/a
37	chr7:78982418-78982468	GM12891	blood:	n/a
38	chr7:78982418-78982468	NHDF-neo	bronchial:	n/a
39	chr7:78982418-78982468	HMEC	breast:	n/a
40	chr7:78982418-78982468	A549	lung:	n/a
41	chr7:78982418-78982468	HCM	heart:	n/a
42	chr7:78982418-78982468	ProgFib	skin:	n/a
43	chr7:78982418-78982468	SAEC	small airway:	n/a
44	chr7:78982418-78982468	AoSMC	blood vessel:	n/a
45	chr7:78982418-78982468	HEEpiC	esophagus:	n/a
46	chr7:78982418-78982468	GM19239	blood:	n/a
47	chr7:78982418-78982468	BE2_C	brain:	n/a
48	chr7:78982418-78982468	SK-N-SH	brain:	n/a
49	chr7:78982418-78982468	HNPCEpiC	eye:	n/a
50	chr7:78982418-78982468	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:79017286..79019685-chr7:79023052..79025297,2	MCF-7	breast:
2	chr7:79011096..79013975-chr7:79014209..79017133,2	MCF-7	breast:
3	chr7:79011096..79013975-chr7:79014209..79017133,2	MCF-7	breast:
4	chr7:79017286..79019685-chr7:79023052..79025297,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNAI1-6	chr7:78982726-78983708	NONHSAT121700

Variant related genes	Relation type
ENSG00000222024	TF binding region
ENSG00000222024	CpG island

Extended variants
information (count: 1556 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1556 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2069132	chr7:78981719-78981720	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs185825382	chr7:78981770-78981771	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs572362412	chr7:78981866-78981867	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs148429290	chr7:78981877-78981878	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs191124182	chr7:78981891-78981892	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs10264527	chr7:78981893-78981894	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs543503713	chr7:78981907-78981908	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs562553072	chr7:78981912-78981913	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs558895070	chr7:78981920-78981921	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs551409024	chr7:78982106-78982107	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs142507541	chr7:78982109-78982110	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs527575793	chr7:78982141-78982142	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs547463665	chr7:78982146-78982147	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs567261382	chr7:78982149-78982150	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs146435100	chr7:78982158-78982159	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs536360590	chr7:78982171-78982172	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs1528259	chr7:78982180-78982181	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs570175132	chr7:78982282-78982283	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs541304625	chr7:78982298-78982299	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs6956190	chr7:78982307-78982308	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs182777687	chr7:78982330-78982331	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs188291111	chr7:78982337-78982338	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs574616607	chr7:78982414-78982415	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs1528282	chr7:78982474-78982475	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs372128126	chr7:78982538-78982539	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs554586780	chr7:78982540-78982541	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs574453883	chr7:78982552-78982553	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs376120088	chr7:78982570-78982571	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs373217234	chr7:78982574-78982575	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs543515404	chr7:78982586-78982587	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs112695456	chr7:78982591-78982592	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs557401135	chr7:78982596-78982597	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs192879662	chr7:78982624-78982625	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs1406166	chr7:78982670-78982671	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs183187966	chr7:78982682-78982683	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs141097306	chr7:78982736-78982737	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs1406165	chr7:78982745-78982746	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs143510500	chr7:78982776-78982777	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs187807447	chr7:78982782-78982783	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs549624845	chr7:78982795-78982796	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs532506828	chr7:78982904-78982905	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs146762270	chr7:78982920-78982921	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs9640776	chr7:78982970-78982971	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs559277172	chr7:78982988-78982989	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs10268915	chr7:78982993-78982994	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs552786036	chr7:78983012-78983013	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs115182159	chr7:78983043-78983044	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs534996736	chr7:78983073-78983074	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs73377244	chr7:78983079-78983080	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs376715366	chr7:78983121-78983122	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Neurodevelopmental disorder	22521361	CNVD
Williams Syndrome	20824207	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Williams-beuren syndrome	16826523	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:156 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78971800-78981800	Weak transcription	Brain Angular Gyrus	brain
2	chr7:78977200-78981800	Weak transcription	Fetal Heart	heart
3	chr7:78980200-78982200	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr7:78980800-78981800	Enhancers	Brain Inferior Temporal Lobe	brain
5	chr7:78980800-78986200	Weak transcription	Brain Substantia Nigra	brain
6	chr7:78981000-78982000	Enhancers	Brain Hippocampus Middle	brain
7	chr7:78981200-78982200	Enhancers	A549	lung
8	chr7:78981400-78982200	Enhancers	Brain Anterior Caudate	brain
9	chr7:78981400-78982200	Enhancers	HepG2	liver
10	chr7:78981600-78982000	Enhancers	NHLF	lung
11	chr7:78981600-78982200	Enhancers	Liver	Liver
12	chr7:78981600-78983000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr7:78981600-78983400	Enhancers	Ovary	ovary
14	chr7:78981800-78982200	Enhancers	Duodenum Smooth Muscle	Duodenum
15	chr7:78981800-78982400	Enhancers	Fetal Heart	heart
16	chr7:78981800-78982600	Enhancers	Brain Cingulate Gyrus	brain
17	chr7:78981800-78983400	Enhancers	Brain Angular Gyrus	brain
18	chr7:78982000-78986000	Weak transcription	Brain Hippocampus Middle	brain
19	chr7:78982000-78992000	Weak transcription	NHLF	lung
20	chr7:78982200-78986000	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr7:78982200-78986200	Weak transcription	Brain Anterior Caudate	brain
22	chr7:78982400-78986400	Weak transcription	Fetal Heart	heart
23	chr7:78982600-78986000	Weak transcription	Brain Cingulate Gyrus	brain
24	chr7:78983000-78985400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr7:78983000-78986600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr7:78983400-78986200	Weak transcription	Brain Angular Gyrus	brain
27	chr7:78986000-78986200	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr7:78986000-78986600	Enhancers	Brain Hippocampus Middle	brain
29	chr7:78986000-78986800	Enhancers	Brain Cingulate Gyrus	brain
30	chr7:78986000-78987000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr7:78986200-78986400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
32	chr7:78986200-78986800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr7:78986200-78986800	Enhancers	Brain Anterior Caudate	brain
34	chr7:78986200-78986800	Enhancers	Brain Substantia Nigra	brain
35	chr7:78986200-78987000	Enhancers	Brain Angular Gyrus	brain
36	chr7:78986400-78986800	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr7:78986400-78987000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr7:78986400-78987000	Enhancers	Fetal Heart	heart
39	chr7:78986600-78986800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr7:78986800-78987000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
41	chr7:78992000-78992400	Enhancers	Liver	Liver
42	chr7:78992000-78992600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr7:78992400-78993400	Weak transcription	Liver	Liver
44	chr7:78993400-78993600	Enhancers	Liver	Liver
45	chr7:78993400-78993800	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr7:79001600-79002000	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr7:79002000-79005800	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr7:79004400-79004600	Enhancers	Brain Substantia Nigra	brain
49	chr7:79005800-79006600	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr7:79005800-79007000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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