Variant report

Variant	nsv1018428
Chromosome Location	chr7:125044642-125730775
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1843)
CpG islands
(count:0)
Chromatin interactive
region (count:111)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1843 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:125238528-125238531	K562	blood:	n/a	n/a
2	ARID3A	chr7:125112702-125112705	K562	blood:	n/a	n/a
3	ARID3A	chr7:125235405-125235419	K562	blood:	n/a	n/a
4	ARID3A	chr7:125145112-125145113	K562	blood:	n/a	n/a
5	ARID3A	chr7:125207883-125208163	K562	blood:	n/a	n/a
6	ARID3A	chr7:125245371-125245822	K562	blood:	n/a	n/a
7	ATF1	chr7:125099017-125099154	K562	blood:	n/a	n/a
8	ATF1	chr7:125304902-125304935	K562	blood:	n/a	n/a
9	ATF1	chr7:125102482-125102530	K562	blood:	n/a	n/a
10	ATF1	chr7:125155568-125155672	K562	blood:	n/a	n/a
11	ATF2	chr7:125606321-125606646	GM12878	blood:	n/a	n/a
12	ATF2	chr7:125208736-125209317	GM12878	blood:	n/a	n/a
13	ATF2	chr7:125208800-125209277	GM12878	blood:	n/a	n/a
14	ATF2	chr7:125292085-125292579	GM12878	blood:	n/a	n/a
15	ATF3	chr7:125245272-125245589	K562	blood:	n/a	n/a
16	BACH1	chr7:125245462-125245548	H1-hESC	embryonic stem cell:	n/a	chr7:125245471-125245485
17	BACH1	chr7:125144864-125145256	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr7:125144988-125145184	K562	blood:	n/a	n/a
19	BACH1	chr7:125250853-125250856	K562	blood:	n/a	n/a
20	BACH1	chr7:125432709-125432803	K562	blood:	n/a	n/a
21	BATF	chr7:125208852-125209217	GM12878	blood:	n/a	n/a
22	BATF	chr7:125400561-125400782	GM12878	blood:	n/a	n/a
23	BATF	chr7:125208879-125209269	GM12878	blood:	n/a	n/a
24	BATF	chr7:125131056-125131238	GM12878	blood:	n/a	n/a
25	BATF	chr7:125463611-125463967	GM12878	blood:	n/a	n/a
26	BATF	chr7:125656888-125657086	GM12878	blood:	n/a	chr7:125657018-125657029 chr7:125657002-125657013
27	BATF	chr7:125144978-125145174	GM12878	blood:	n/a	chr7:125145074-125145085
28	BATF	chr7:125444374-125444778	GM12878	blood:	n/a	n/a
29	BCL11A	chr7:125444389-125444708	GM12878	blood:	n/a	n/a
30	BCL11A	chr7:125208879-125209307	GM12878	blood:	n/a	n/a
31	BCL11A	chr7:125208927-125209202	GM12878	blood:	n/a	n/a
32	BCL3	chr7:125460885-125461181	GM12878	blood:	n/a	n/a
33	BCL3	chr7:125208897-125209206	GM12878	blood:	n/a	n/a
34	BCL3	chr7:125292138-125292574	GM12878	blood:	n/a	n/a
35	BCLAF1	chr7:125208811-125209257	GM12878	blood:	n/a	n/a
36	BCLAF1	chr7:125208875-125209224	GM12878	blood:	n/a	n/a
37	BHLHE40	chr7:125301808-125302109	K562	blood:	n/a	n/a
38	BHLHE40	chr7:125052988-125053632	GM12878	blood:	n/a	n/a
39	BHLHE40	chr7:125208861-125209208	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:125315765-125315880	K562	blood:	n/a	n/a
41	BHLHE40	chr7:125375284-125375348	K562	blood:	n/a	n/a
42	BHLHE40	chr7:125178945-125179203	K562	blood:	n/a	chr7:125179077-125179098 chr7:125179081-125179094
43	BHLHE40	chr7:125720305-125720422	GM12878	blood:	n/a	n/a
44	BHLHE40	chr7:125242283-125242313	K562	blood:	n/a	n/a
45	BHLHE40	chr7:125201165-125201410	GM12878	blood:	n/a	n/a
46	BRCA1	chr7:125311175-125311315	H1-hESC	embryonic stem cell:	n/a	n/a
47	BRCA1	chr7:125661964-125662015	H1-hESC	embryonic stem cell:	n/a	n/a
48	BRCA1	chr7:125131722-125131738	GM12878	blood:	n/a	n/a
49	CBX3	chr7:125377948-125378165	K562	blood:	n/a	n/a
50	CBX3	chr7:125574517-125575153	HCT-116	colon:	n/a	n/a

No data

(count:111 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:125070959..125073239-chr7:125075739..125078658,3	K562	blood:
2	chr7:125204110..125205826-chr7:125284105..125286281,2	K562	blood:
3	chr7:125023517..125024026-chr7:125310752..125311652,2	MCF-7	breast:
4	chr7:125384743..125387377-chr7:125395816..125398229,2	K562	blood:
5	chr7:125459178..125461778-chr7:125471242..125473065,2	K562	blood:
6	chr7:125172761..125175135-chr7:125186431..125188601,2	K562	blood:
7	chr7:125325822..125328394-chr7:125330208..125331998,2	K562	blood:
8	chr7:125205327..125207901-chr7:125208820..125211664,2	K562	blood:
9	chr7:124699558..124701618-chr7:125055753..125057701,2	K562	blood:
10	chr7:125251686..125253446-chr7:125261235..125263882,2	K562	blood:
11	chr7:125338629..125340672-chr7:125343129..125344648,2	K562	blood:
12	chr7:125458557..125461124-chr7:125464853..125467696,3	K562	blood:
13	chr7:125241383..125243841-chr7:125245305..125247119,2	K562	blood:
14	chr7:125218658..125220340-chr7:125222287..125223970,2	K562	blood:
15	chr7:125598344..125601168-chr7:125601374..125603496,2	K562	blood:
16	chr7:125234853..125237677-chr7:125237685..125240938,4	K562	blood:
17	chr7:125298032..125299556-chr7:125301749..125304185,2	K562	blood:
18	chr7:125125355..125128224-chr7:125131443..125135163,4	K562	blood:
19	chr7:125190321..125191930-chr7:125194449..125196273,2	K562	blood:
20	chr7:125480828..125483147-chr7:125484662..125486648,3	K562	blood:
21	chr7:125269070..125270794-chr7:125275616..125278202,2	K562	blood:
22	chr7:125083153..125085780-chr7:125088082..125089929,2	K562	blood:
23	chr7:125241383..125243591-chr7:125245619..125247438,2	K562	blood:
24	chr7:125298032..125299556-chr7:125301749..125304185,2	K562	blood:
25	chr7:125449848..125452738-chr7:125466258..125468115,2	K562	blood:
26	chr7:125190321..125191930-chr7:125194449..125196273,2	K562	blood:
27	chr7:125458557..125461124-chr7:125464853..125467696,3	K562	blood:
28	chr7:125226088..125228401-chr7:125230345..125233728,3	K562	blood:
29	chr7:125385463..125387105-chr7:125388625..125390168,2	K562	blood:
30	chr7:125414524..125416692-chr7:125417841..125420169,2	K562	blood:
31	chr7:125385605..125387936-chr7:125388625..125390972,2	K562	blood:
32	chr7:125503485..125505838-chr7:125510638..125513517,2	K562	blood:
33	chr7:125392984..125395323-chr7:125485232..125486912,2	K562	blood:
34	chr7:125280203..125282931-chr7:125290069..125292178,2	K562	blood:
35	chr7:125251686..125253446-chr7:125261235..125263882,2	K562	blood:
36	chr7:125310080..125313010-chr7:125315945..125318441,2	K562	blood:
37	chr7:125683918..125686254-chr7:125689679..125692270,2	K562	blood:
38	chr7:125459178..125461778-chr7:125471242..125473065,2	K562	blood:
39	chr7:125620692..125622990-chr7:125623881..125626292,2	K562	blood:
40	chr7:125271199..125273030-chr7:125279444..125281182,2	K562	blood:
41	chr7:125241383..125243591-chr7:125245619..125247438,2	K562	blood:
42	chr7:125125355..125128224-chr7:125131443..125135163,4	K562	blood:
43	chr7:125089598..125092751-chr7:125096828..125101024,3	K562	blood:
44	chr7:125574020..125576631-chr7:125579427..125582036,2	K562	blood:
45	chr7:125369632..125371193-chr7:125372789..125375510,2	K562	blood:
46	chr7:125266350..125268456-chr7:125268990..125271512,2	K562	blood:
47	chr7:125243932..125247685-chr7:125249366..125252787,4	K562	blood:
48	chr7:125574020..125576631-chr7:125579427..125582036,2	K562	blood:
49	chr7:125235978..125238946-chr7:125246634..125248463,2	K562	blood:
50	chr7:124846681..124848535-chr7:125206338..125208006,2	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPAM1-6	chr7:125101535-125101923	ENSG00000227869
2	lnc-SPAM1-6	chr7:125101535-125101704	ENSG00000227869
3	lnc-SPAM1-6	chr7:125078165-125078351	ENSG00000227869
4	lnc-SPAM1-6	chr7:125071401-125071647	ENSG00000227869
5	lnc-SPAM1-6	chr7:125101535-125101665	ENSG00000227869
6	lnc-SPAM1-6	chr7:125078199-125078351	ENSG00000227869
7	lnc-SPAM1-6	chr7:125106324-125106455	NONHSAT123109
8	lnc-SPAM1-6	chr7:125078165-125078351	NONHSAT123109
9	lnc-SPAM1-6	chr7:125071401-125071647	NONHSAT123109
10	lnc-ARF5-6	chr7:125560111-125560207	XLOC_006234
11	lnc-ARF5-6	chr7:125573828-125573886	XLOC_006234
12	lnc-SPAM1-6	chr7:125078276-125078351	ENSG00000227869
13	lnc-ARF5-6	chr7:125563748-125564004	XLOC_006234
14	lnc-SPAM1-6	chr7:125106324-125106455	ENSG00000227869
15	lnc-ARF5-6	chr7:125557925-125558172	XLOC_006234
16	lnc-SPAM1-6	chr7:125101535-125101923	NONHSAT123109
17	lnc-ARF5-6	chr7:125564266-125564441	XLOC_006234

No data

Variant related genes	Relation type
ENSG00000227869	TF binding region
ENSG00000221418	TF binding region
ENSG00000197462	TF binding region
ENSG00000201801	chromatin interactions
ENSG00000227869	chromatin interactions
ENSG00000107281	chromatin interactions
ENSG00000199347	chromatin interactions

Extended variants
information (count: 13491 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:13491 , 50 per page) page: 1 2 3 4 5 6 7 ... 270

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183334979	chr7:125045408-125045409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs1526408	chr7:125045427-125045428	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs75426046	chr7:125045463-125045464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs553297936	chr7:125045481-125045482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs142987353	chr7:125045490-125045491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs116279784	chr7:125045498-125045499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150661848	chr7:125045554-125045555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs117324738	chr7:125045555-125045556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543923271	chr7:125045560-125045561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560984130	chr7:125045587-125045588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs529646515	chr7:125045644-125045645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140958479	chr7:125045659-125045660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187283700	chr7:125045716-125045717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs553583747	chr7:125045719-125045720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115463754	chr7:125045726-125045727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs57140942	chr7:125045776-125045777	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs531039753	chr7:125045877-125045878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550795644	chr7:125045908-125045909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs144299449	chr7:125045949-125045950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558757797	chr7:125045951-125045952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536239604	chr7:125045989-125045990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553372938	chr7:125045999-125046000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369420381	chr7:125046003-125046004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs397817076	chr7:125046011-125046012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192120404	chr7:125046028-125046029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568594092	chr7:125046039-125046040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376144291	chr7:125046042-125046043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182814573	chr7:125046129-125046130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544236068	chr7:125046132-125046133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563668295	chr7:125046161-125046162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs114626716	chr7:125046179-125046180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs115645601	chr7:125046191-125046192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188437332	chr7:125046204-125046205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs544334374	chr7:125046267-125046268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554351395	chr7:125046281-125046282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs71576235	chr7:125046303-125046304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs34545654	chr7:125046355-125046356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs192227487	chr7:125046373-125046374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs77115498	chr7:125046374-125046375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529270752	chr7:125046458-125046459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs114964846	chr7:125046462-125046463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545250872	chr7:125046474-125046475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs565522539	chr7:125046486-125046487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs11772320	chr7:125046525-125046526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs531004235	chr7:125046529-125046530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs551091345	chr7:125046554-125046555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs184611393	chr7:125046586-125046587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs573847966	chr7:125046659-125046660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs6467009	chr7:125046708-125046709	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs188335547	chr7:125046750-125046751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Autism	22495311	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
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	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
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	21635232	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Autism	20858243	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Autism	19246517	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:125045400-125045600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:125045600-125050400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:125046200-125046600	Enhancers	HUVEC	blood vessel
4	chr7:125049600-125050400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:125049800-125050000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr7:125049800-125050600	Enhancers	HMEC	breast
7	chr7:125050000-125053600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr7:125050400-125050800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr7:125050400-125059600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr7:125053000-125053800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr7:125053200-125053600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr7:125053400-125053800	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr7:125053600-125054400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr7:125055000-125055400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr7:125055400-125056800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr7:125056800-125058600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr7:125059600-125060200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr7:125060200-125063200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr7:125063000-125065000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr7:125063200-125063800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr7:125063200-125065200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr7:125063200-125065800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr7:125063400-125063800	Enhancers	Primary hematopoietic stem cells	blood
24	chr7:125063400-125064000	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr7:125063400-125064800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr7:125063400-125065400	Enhancers	HUVEC	blood vessel
27	chr7:125063400-125065800	Enhancers	HMEC	breast
28	chr7:125063800-125067000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr7:125064000-125064400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr7:125064400-125065000	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr7:125064400-125065000	Enhancers	NHEK	skin
32	chr7:125064400-125065400	Enhancers	Hela-S3	cervix
33	chr7:125064800-125067000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr7:125065400-125067800	Weak transcription	HUVEC	blood vessel
35	chr7:125065600-125066000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr7:125065800-125067000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr7:125065800-125078000	Weak transcription	HMEC	breast
38	chr7:125066400-125067200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr7:125067000-125067200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr7:125067000-125067400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr7:125067000-125067800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr7:125067000-125068200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr7:125067200-125067600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr7:125067400-125068400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr7:125067600-125069200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr7:125067800-125068000	ZNF genes & repeats	HUVEC	blood vessel
47	chr7:125067800-125068200	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr7:125068200-125086200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr7:125068400-125068600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr7:125069200-125070600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links