Variant report

Variant	nsv970964
Chromosome Location	chr7:149692674-149761173
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	ATF1	chr7:149742080-149742094	K562	blood:	n/a	n/a
2	ATF1	chr7:149700297-149700734	K562	blood:	n/a	n/a
3	BACH1	chr7:149746378-149746646	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr7:149743485-149743750	GM12878	blood:	n/a	n/a
5	BATF	chr7:149757655-149757938	GM12878	blood:	n/a	chr7:149757827-149757838
6	CEBPB	chr7:149701346-149701464	A549	lung:	n/a	n/a
7	CEBPB	chr7:149701451-149701643	IMR90	lung:	n/a	n/a
8	CEBPB	chr7:149713771-149714042	HepG2	liver:	n/a	n/a
9	CEBPB	chr7:149701434-149701491	K562	blood:	n/a	n/a
10	CHD1	chr7:149746398-149746684	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr7:149746382-149746488	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr7:149757620-149757770	HEK293	kidney:	n/a	n/a
13	CTCF	chr7:149742800-149742950	HCPEpiC	choroid plexus:	n/a	n/a
14	CTCF	chr7:149757632-149757914	K562	blood:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
15	CTCF	chr7:149698380-149698530	SK-N-SH_RA	brain:	n/a	n/a
16	CTCF	chr7:149757633-149757915	Pancreas_OC	pancreas:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
17	CTCF	chr7:149742754-149743021	K562	blood:	n/a	n/a
18	CTCF	chr7:149757660-149757810	HCM	heart:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
19	CTCF	chr7:149757660-149757810	BE2_C	brain:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
20	CTCF	chr7:149757660-149757810	NHLF	lung:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
21	CTCF	chr7:149745917-149746469	K562	blood:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
22	CTCF	chr7:149757660-149757810	HAc	cerebellar:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
23	CTCF	chr7:149722314-149722427	GM12892	blood:	n/a	chr7:149722360-149722381 chr7:149722365-149722383
24	CTCF	chr7:149698297-149698558	A549	lung:	n/a	n/a
25	CTCF	chr7:149698428-149698565	HepG2	liver:	n/a	n/a
26	CTCF	chr7:149757620-149757770	HRE	kidney:	n/a	n/a
27	CTCF	chr7:149742800-149742950	NB4	blood:	n/a	n/a
28	CTCF	chr7:149742487-149743058	SK-N-SH	brain:	n/a	n/a
29	CTCF	chr7:149745900-149746050	Caco-2	colon:	n/a	n/a
30	CTCF	chr7:149757620-149757770	AG10803	skin:	n/a	n/a
31	CTCF	chr7:149746051-149746369	GM12891	blood:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
32	CTCF	chr7:149757284-149757527	GM13976	blood:	n/a	n/a
33	CTCF	chr7:149746116-149746319	GM19239	blood:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
34	CTCF	chr7:149757602-149757958	A549	lung:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
35	CTCF	chr7:149757427-149757488	GM10266	blood:	n/a	n/a
36	CTCF	chr7:149743548-149743581	GM12891	blood:	n/a	n/a
37	CTCF	chr7:149742700-149742850	BE2_C	brain:	n/a	n/a
38	CTCF	chr7:149757561-149757916	A549	lung:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
39	CTCF	chr7:149749352-149749448	LNCaP	prostate:	n/a	chr7:149749391-149749400
40	CTCF	chr7:149757620-149757770	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr7:149746320-149746590	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr7:149742840-149742990	A549	lung:	n/a	n/a
43	CTCF	chr7:149757660-149757810	GM12872	blood:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
44	CTCF	chr7:149757649-149757902	MCF-7	breast:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
45	CTCF	chr7:149742780-149742930	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr7:149722202-149722480	A549	lung:	n/a	chr7:149722360-149722381 chr7:149722365-149722383
47	CTCF	chr7:149757620-149757770	GM12872	blood:	n/a	n/a
48	CTCF	chr7:149704792-149704816	LNCaP	prostate:	n/a	n/a
49	CTCF	chr7:149746153-149746320	GM10266	blood:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
50	CTCF	chr7:149742790-149743004	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:149742121-149742171	HCPEpiC	choroid plexus:	n/a
2	chr7:149742121-149742171	HCPEpiC	choroid plexus:	n/a
3	chr7:149734481-149734531	HCPEpiC	choroid plexus:	n/a
4	chr7:149742121-149742171	PFSK-1	brain:	n/a
5	chr7:149732847-149732897	HUVEC	blood vessel:	n/a
6	chr7:149738501-149738551	SKMC	muscle:	n/a
7	chr7:149736127-149736177	T-47D	breast:	n/a
8	chr7:149746468-149746518	GM19239	blood:	n/a
9	chr7:149732847-149732897	BJ	skin:	n/a
10	chr7:149746640-149746690	ECC-1	luminal epithelium:	n/a
11	chr7:149732847-149732897	NHDF-neo	bronchial:	n/a
12	chr7:149744935-149744985	Hepatocyte	liver:	n/a
13	chr7:149738473-149738523	NT2-D1	testis:	n/a
14	chr7:149746468-149746518	HRCEpiC	kidney:	n/a
15	chr7:149745299-149745349	MCF10A-Er-Src	breast:	n/a
16	chr7:149744041-149744091	A549	lung:	n/a
17	chr7:149746077-149746127	H1-hESC	embryonic stem cell:	embryo
18	chr7:149736127-149736177	AG10803	skin:	n/a
19	chr7:149746640-149746690	NHBE	bronchial:	n/a
20	chr7:149746077-149746127	MCF-7	breast:	n/a
21	chr7:149733103-149733153	SK-N-SH	brain:	n/a
22	chr7:149732847-149732897	AG04449	skin:	fetal
23	chr7:149744597-149744647	K562	blood:	n/a
24	chr7:149749941-149749991	CMK	blood:	n/a
25	chr7:149735726-149735776	ovcar-3	ovarian:	n/a
26	chr7:149735726-149735776	MCF-7	breast:	n/a
27	chr7:149744418-149744468	AG04450	lung:	fetal
28	chr7:149746640-149746690	HAEpiC	amniotic membrane:	n/a
29	chr7:149735726-149735776	SK-N-MC	brain:	n/a
30	chr7:149734481-149734531	H1-hESC	embryonic stem cell:	embryo
31	chr7:149735726-149735776	HCF	heart:	n/a
32	chr7:149735726-149735776	T-47D	breast:	n/a
33	chr7:149735729-149735779	HUVEC	blood vessel:	n/a
34	chr7:149738473-149738523	IMR90	lung:	fetal
35	chr7:149744597-149744647	HCT-116	colon:	n/a
36	chr7:149732579-149732629	SAEC	small airway:	n/a
37	chr7:149735726-149735776	CMK	blood:	n/a
38	chr7:149733103-149733153	MCF10A-Er-Src	breast:	n/a
39	chr7:149733103-149733153	AG04450	lung:	fetal
40	chr7:149746640-149746690	ProgFib	skin:	n/a
41	chr7:149744418-149744468	HRPEpiC	eye:	n/a
42	chr7:149744418-149744468	GM06990	blood:	n/a
43	chr7:149746468-149746518	NHDF-neo	bronchial:	n/a
44	chr7:149746468-149746518	HIPEpiC	eye:	n/a
45	chr7:149749941-149749991	GM12892	blood:	n/a
46	chr7:149738473-149738523	AoSMC	blood vessel:	n/a
47	chr7:149738501-149738551	AoSMC	blood vessel:	n/a
48	chr7:149731742-149731792	GM19239	blood:	n/a
49	chr7:149744597-149744647	HMEC	breast:	n/a
50	chr7:149746468-149746518	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:149699024..149700856-chr7:153788710..153791500,2	K562	blood:
2	chr7:149580322..149580844-chr7:149745955..149746566,2	MCF-7	breast:
3	chr7:149757556..149758057-chr7:149919306..149919858,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP6V0E2-2	chr7:149732185-149732207	NONHSAT124087
2	lnc-ATP6V0E2-1	chr7:149697841-149700167	ENSG00000249583
3	lnc-ATP6V0E2-2	chr7:149737556-149737743	NONHSAT124091
4	lnc-ZNF467-4	chr7:149700614-149701513	NONHSAT124086
5	lnc-ATP6V0E2-2	chr7:149741839-149742195	NONHSAT124091
6	lnc-ATP6V0E2-2	chr7:149738452-149738550	NONHSAT124091
7	lnc-ATP6V0E2-2	chr7:149738452-149738550	ENSG00000241449
8	lnc-ATP6V0E2-2	chr7:149741839-149742195	NONHSAT124088
9	lnc-ZNF467-4	chr7:149699986-149700449	NONHSAT124086
10	lnc-ATP6V0E2-2	chr7:149735636-149735802	NONHSAT124088
11	lnc-ATP6V0E2-1	chr7:149701497-149702213	ENSG00000249583
12	lnc-ATP6V0E2-2	chr7:149737610-149737743	ENSG00000241449
13	lnc-ATP6V0E2-8	chr7:149697081-149697368	expReg_chr7_12098_+
14	lnc-ATP6V0E2-2	chr7:149741839-149742195	NONHSAT124087
15	lnc-ATP6V0E2-2	chr7:149759178-149759348	ENSG00000241449

Variant related genes	Relation type
ENSG00000241449	TF binding region
ENSG00000260555	TF binding region
ENSG00000241449	CpG island
ENSG00000260555	CpG island
JPH1	miRNA target sites
SOCS2	miRNA target sites

Extended variants
information (count: 3184 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:3184 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368538256	chr7:149692693-149692694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs534481703	chr7:149692697-149692698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547445255	chr7:149692699-149692700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570375994	chr7:149692727-149692728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539387914	chr7:149692756-149692757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555998425	chr7:149692757-149692758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs13230736	chr7:149692792-149692793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs34718531	chr7:149692824-149692825	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569688295	chr7:149692828-149692829	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535314392	chr7:149692834-149692835	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555130996	chr7:149692837-149692838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs115232222	chr7:149692876-149692877	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs115224735	chr7:149692882-149692883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184423685	chr7:149692893-149692894	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558001680	chr7:149692913-149692914	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577183964	chr7:149692920-149692921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546138695	chr7:149692942-149692943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562843116	chr7:149692944-149692945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs202216192	chr7:149692966-149692967	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372197862	chr7:149692989-149692990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558264877	chr7:149692990-149692991	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531838799	chr7:149693030-149693031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542477196	chr7:149693036-149693037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201537056	chr7:149693072-149693073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200531540	chr7:149693097-149693098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs35703257	chr7:149693138-149693139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs199586070	chr7:149693139-149693140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562246265	chr7:149693227-149693228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527858953	chr7:149693251-149693252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547791006	chr7:149693260-149693261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188411283	chr7:149693261-149693262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532795747	chr7:149693284-149693285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs146176444	chr7:149693288-149693289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569693820	chr7:149693312-149693313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535161471	chr7:149693313-149693314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555169638	chr7:149693327-149693328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565557878	chr7:149693506-149693507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534474078	chr7:149693560-149693561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552517754	chr7:149693606-149693607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375696329	chr7:149693609-149693610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575088496	chr7:149693634-149693635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572994892	chr7:149693667-149693668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368052665	chr7:149693671-149693672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201208752	chr7:149693675-149693676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs199864968	chr7:149693682-149693683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191615742	chr7:149693703-149693704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557776764	chr7:149693772-149693773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577822243	chr7:149693804-149693805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs142902124	chr7:149693935-149693936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201689218	chr7:149693967-149693968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:502 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:149688600-149696000	Weak transcription	Gastric	stomach
2	chr7:149692000-149700600	Weak transcription	Right Atrium	heart
3	chr7:149692600-149700400	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr7:149692800-149693000	Enhancers	Brain Angular Gyrus	brain
5	chr7:149693000-149700400	Weak transcription	Brain Angular Gyrus	brain
6	chr7:149694800-149700200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr7:149694800-149700400	Weak transcription	Ovary	ovary
8	chr7:149696000-149696200	Enhancers	Brain Anterior Caudate	brain
9	chr7:149696000-149696600	Enhancers	Gastric	stomach
10	chr7:149696200-149698000	Weak transcription	Pancreas	Pancrea
11	chr7:149696200-149700400	Weak transcription	Brain Anterior Caudate	brain
12	chr7:149696600-149700400	Weak transcription	Gastric	stomach
13	chr7:149697800-149698600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr7:149698000-149698200	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr7:149698000-149698200	Enhancers	Pancreas	Pancrea
16	chr7:149698200-149700400	Weak transcription	Pancreas	Pancrea
17	chr7:149698400-149702000	Weak transcription	Brain Hippocampus Middle	brain
18	chr7:149698600-149700400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr7:149698800-149700400	Weak transcription	Brain Cingulate Gyrus	brain
20	chr7:149698800-149700400	Weak transcription	Colon Smooth Muscle	Colon
21	chr7:149699000-149700400	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr7:149699000-149700800	Weak transcription	Fetal Brain Female	brain
23	chr7:149699200-149704000	Weak transcription	Liver	Liver
24	chr7:149699800-149701200	Weak transcription	HepG2	liver
25	chr7:149700000-149700400	Weak transcription	Brain Substantia Nigra	brain
26	chr7:149700200-149700400	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr7:149700200-149700600	Weak transcription	Colonic Mucosa	Colon
28	chr7:149700200-149701000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
29	chr7:149700200-149701000	ZNF genes & repeats	Fetal Brain Male	brain
30	chr7:149700200-149701000	ZNF genes & repeats	Fetal Kidney	kidney
31	chr7:149700400-149700600	Enhancers	Right Ventricle	heart
32	chr7:149700400-149700600	Bivalent/Poised TSS	Stomach Mucosa	stomach
33	chr7:149700400-149700600	Bivalent Enhancer	K562	blood
34	chr7:149700400-149700800	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
35	chr7:149700400-149700800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
36	chr7:149700400-149700800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
37	chr7:149700400-149700800	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
38	chr7:149700400-149700800	ZNF genes & repeats	Fetal Heart	heart
39	chr7:149700400-149700800	ZNF genes & repeats	Fetal Intestine Large	intestine
40	chr7:149700400-149700800	ZNF genes & repeats	Ovary	ovary
41	chr7:149700400-149700800	Active TSS	NHDF-Ad	bronchial
42	chr7:149700400-149701000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
43	chr7:149700400-149701000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr7:149700400-149701000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr7:149700400-149701000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr7:149700400-149701000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
47	chr7:149700400-149701000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr7:149700400-149701000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr7:149700400-149701000	Strong transcription	Brain Angular Gyrus	brain
50	chr7:149700400-149701000	Strong transcription	Brain Anterior Caudate	brain

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