Variant report

Variant	nsv881606
Chromosome Location	chr4:171640683-171760509
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:343)
CpG islands
(count:122)
Chromatin interactive
region (count:10)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:343 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr4:171691065-171691307	K562	blood:	n/a	n/a
2	CEBPB	chr4:171748396-171748675	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr4:171644369-171644648	HepG2	liver:	n/a	chr4:171644495-171644506
4	CEBPB	chr4:171694122-171694374	H1-hESC	embryonic stem cell:	n/a	chr4:171694220-171694231
5	CEBPB	chr4:171694076-171694414	Hela-S3	cervix:	n/a	chr4:171694220-171694231
6	CEBPB	chr4:171749009-171749469	Hela-S3	cervix:	n/a	chr4:171749275-171749288 chr4:171749277-171749288 chr4:171749277-171749288
7	CEBPB	chr4:171694052-171694390	HepG2	liver:	n/a	chr4:171694220-171694231
8	CEBPB	chr4:171760418-171760618	A549	lung:	n/a	n/a
9	CTCF	chr4:171760500-171760650	NHEK	skin:	n/a	chr4:171760538-171760546
10	CTCF	chr4:171726620-171726770	HepG2	liver:	n/a	n/a
11	CTCF	chr4:171671780-171671930	HepG2	liver:	n/a	chr4:171671861-171671879
12	CTCF	chr4:171726659-171726805	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr4:171671740-171671890	A549	lung:	n/a	chr4:171671861-171671879
14	CTCF	chr4:171671800-171671950	SK-N-SH_RA	brain:	n/a	chr4:171671861-171671879
15	CTCF	chr4:171671820-171671970	BE2_C	brain:	n/a	chr4:171671861-171671879
16	CTCF	chr4:171735400-171735550	GM06990	blood:	n/a	n/a
17	CTCF	chr4:171726580-171726730	A549	lung:	n/a	n/a
18	CTCF	chr4:171671960-171672110	GM12871	blood:	n/a	n/a
19	CTCF	chr4:171671834-171671877	GM19239	blood:	n/a	n/a
20	CTCF	chr4:171671760-171671910	MCF-7	breast:	n/a	chr4:171671861-171671879
21	CTCF	chr4:171726651-171726833	MCF-7	breast:	n/a	n/a
22	CTCF	chr4:171697837-171697871	MCF-7	breast:	n/a	n/a
23	CTCF	chr4:171671853-171671879	GM19238	blood:	n/a	chr4:171671861-171671879
24	CTCF	chr4:171760500-171760650	HMEC	breast:	n/a	chr4:171760538-171760546
25	CTCF	chr4:171671800-171671950	GM12873	blood:	n/a	chr4:171671861-171671879
26	CTCF	chr4:171671780-171671930	GM12872	blood:	n/a	chr4:171671861-171671879
27	CTCF	chr4:171671740-171671890	GM12865	blood:	n/a	chr4:171671861-171671879
28	CTCF	chr4:171678004-171678038	MCF-7	breast:	n/a	n/a
29	CTCF	chr4:171671760-171671910	GM12869	blood:	n/a	chr4:171671861-171671879
30	CTCF	chr4:171671840-171671990	GM06990	blood:	n/a	chr4:171671861-171671879
31	CTCF	chr4:171671829-171671891	GM13977	blood:	n/a	chr4:171671861-171671879
32	CTCF	chr4:171726537-171726860	MCF-7	breast:	n/a	n/a
33	CTCF	chr4:171726680-171726830	MCF-7	breast:	n/a	n/a
34	CTCF	chr4:171726655-171726840	MCF-7	breast:	n/a	n/a
35	CTCF	chr4:171671780-171671930	GM12865	blood:	n/a	chr4:171671861-171671879
36	CTCF	chr4:171671732-171671977	MCF-7	breast:	n/a	chr4:171671861-171671879
37	CTCF	chr4:171729360-171729510	GM06990	blood:	n/a	n/a
38	CTCF	chr4:171671800-171671918	HepG2	liver:	n/a	chr4:171671861-171671879
39	CTCF	chr4:171760489-171760592	GM12878	blood:	n/a	chr4:171760538-171760546
40	CTCF	chr4:171726635-171726638	MCF-7	breast:	n/a	n/a
41	CTCF	chr4:171671773-171671968	MCF-7	breast:	n/a	chr4:171671861-171671879
42	CTCF	chr4:171677940-171678090	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:171726620-171726770	HEK293	kidney:	n/a	n/a
44	CTCF	chr4:171671775-171671880	SK-N-SH_RA	brain:	n/a	chr4:171671861-171671879
45	CTCF	chr4:171671753-171671977	MCF-7	breast:	n/a	chr4:171671861-171671879
46	CTCF	chr4:171726769-171726780	HepG2	liver:	n/a	n/a
47	CTCF	chr4:171671690-171672027	MCF-7	breast:	n/a	chr4:171671861-171671879
48	CTCF	chr4:171671740-171671890	HVMF	connective:	n/a	chr4:171671861-171671879
49	CTCF	chr4:171671780-171671950	MCF-7	breast:	n/a	chr4:171671861-171671879
50	CTCF	chr4:171726639-171726704	Medullo	brain:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:171709862-171709912	A549	lung:	n/a
2	chr4:171663610-171663660	HCT-116	colon:	n/a
3	chr4:171663610-171663660	NHBE	bronchial:	n/a
4	chr4:171709862-171709912	HMEC	breast:	n/a
5	chr4:171709862-171709912	Hepatocyte	liver:	n/a
6	chr4:171663610-171663660	HCM	heart:	n/a
7	chr4:171709862-171709912	T-47D	breast:	n/a
8	chr4:171709862-171709912	LNCaP	prostate:	n/a
9	chr4:171663610-171663660	ProgFib	skin:	n/a
10	chr4:171709862-171709912	GM12878	blood:	n/a
11	chr4:171709862-171709912	SK-N-SH	brain:	n/a
12	chr4:171663610-171663660	HPAEpiC	pulmonary alveolar:	n/a
13	chr4:171709862-171709912	PrEC	prostate:	n/a
14	chr4:171663610-171663660	GM12878	blood:	n/a
15	chr4:171663610-171663660	HUVEC	blood vessel:	n/a
16	chr4:171663610-171663660	GM12892	blood:	n/a
17	chr4:171663610-171663660	PFSK-1	brain:	n/a
18	chr4:171709862-171709912	ECC-1	luminal epithelium:	n/a
19	chr4:171709862-171709912	ovcar-3	ovarian:	n/a
20	chr4:171663610-171663660	AG04450	lung:	fetal
21	chr4:171663610-171663660	HAEpiC	amniotic membrane:	n/a
22	chr4:171709862-171709912	IMR90	lung:	fetal
23	chr4:171709862-171709912	PANC-1	pancreas:	n/a
24	chr4:171709862-171709912	SKMC	muscle:	n/a
25	chr4:171663610-171663660	AG09319	gingival:	n/a
26	chr4:171663610-171663660	HRCEpiC	kidney:	n/a
27	chr4:171709862-171709912	GM12892	blood:	n/a
28	chr4:171709862-171709912	CMK	blood:	n/a
29	chr4:171663610-171663660	HepG2	liver:	n/a
30	chr4:171663610-171663660	SK-N-SH	brain:	n/a
31	chr4:171709862-171709912	AoSMC	blood vessel:	n/a
32	chr4:171663610-171663660	AG04449	skin:	fetal
33	chr4:171709862-171709912	RPTEC	kidney:	n/a
34	chr4:171709862-171709912	HPAEpiC	pulmonary alveolar:	n/a
35	chr4:171663610-171663660	CMK	blood:	n/a
36	chr4:171663610-171663660	HEK293	kidney:	embryo
37	chr4:171663610-171663660	ovcar-3	ovarian:	n/a
38	chr4:171663610-171663660	AG09309	skin:	n/a
39	chr4:171663610-171663660	NT2-D1	testis:	n/a
40	chr4:171709862-171709912	HEEpiC	esophagus:	n/a
41	chr4:171663610-171663660	SK-N-SH_RA	brain:	n/a
42	chr4:171709862-171709912	AG04449	skin:	fetal
43	chr4:171663610-171663660	HCF	heart:	n/a
44	chr4:171663610-171663660	GM06990	blood:	n/a
45	chr4:171663610-171663660	Hepatocyte	liver:	n/a
46	chr4:171663610-171663660	AoSMC	blood vessel:	n/a
47	chr4:171709862-171709912	HCT-116	colon:	n/a
48	chr4:171663610-171663660	HRPEpiC	eye:	n/a
49	chr4:171663610-171663660	SAEC	small airway:	n/a
50	chr4:171663610-171663660	HRE	kidney:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:171739438..171741940-chr4:171744018..171745762,2	K562	blood:
2	chr4:171718644..171721578-chr4:171722752..171725551,2	K562	blood:
3	chr4:171755644..171758176-chr4:171761937..171764529,2	MCF-7	breast:
4	chr4:171722091..171723639-chr4:171731576..171734168,2	MCF-7	breast:
5	chr4:171671477..171672293-chr4:171774330..171775293,5	MCF-7	breast:
6	chr4:171718644..171721578-chr4:171722752..171725551,2	K562	blood:
7	chr4:171742755..171745728-chr4:171748600..171750384,2	MCF-7	breast:
8	chr4:171742755..171745728-chr4:171748600..171750384,2	MCF-7	breast:
9	chr4:171722091..171723639-chr4:171731576..171734168,2	MCF-7	breast:
10	chr4:171739438..171741940-chr4:171744018..171745762,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AADAT-3	chr4:171664816-171664869	XLOC_004157
2	lnc-AADAT-3	chr4:171663620-171664179	XLOC_004157
3	lnc-AADAT-11	chr4:171735490-171735699	NONHSAT099191
4	lnc-AADAT-3	chr4:171663302-171663311	NONHSAT099189
5	lnc-AADAT-3	chr4:171663746-171664179	NONHSAT099189
6	lnc-AADAT-3	chr4:171664816-171664886	NONHSAT099189

No data

Variant related genes	Relation type
ENSG00000249943	TF binding region
ENSG00000250968	TF binding region
ENSG00000249943	CpG island
ENSG00000250968	CpG island
KEAP1	miRNA target sites
KHSRP	miRNA target sites

Extended variants
information (count: 1389 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1389 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1403211	chr4:171640683-171640684	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533262268	chr4:171640697-171640698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551776974	chr4:171640705-171640706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566734710	chr4:171640740-171640741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs114495705	chr4:171640742-171640743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs186943133	chr4:171640785-171640786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs190176803	chr4:171640816-171640817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs556927148	chr4:171640820-171640821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs555720375	chr4:171640839-171640840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs145156808	chr4:171640868-171640869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs538047094	chr4:171640892-171640893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs78486080	chr4:171640896-171640897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs79852116	chr4:171640898-171640899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556076360	chr4:171640909-171640910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs34635330	chr4:171640910-171640911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs577716443	chr4:171640912-171640913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544755756	chr4:171640916-171640917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs397800829	chr4:171640918-171640919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553766290	chr4:171640919-171640920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571727162	chr4:171641048-171641049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs537615931	chr4:171641068-171641069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542189871	chr4:171641074-171641075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs369584475	chr4:171641110-171641111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs562049426	chr4:171641127-171641128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549928238	chr4:171641157-171641158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs17056044	chr4:171641176-171641177	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs17056046	chr4:171641180-171641181	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs138979914	chr4:171641201-171641202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10520189	chr4:171641235-171641236	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs1996831	chr4:171641250-171641251	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs368890820	chr4:171641252-171641253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377476501	chr4:171641273-171641274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs185838794	chr4:171641312-171641313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs114844042	chr4:171641358-171641359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189719614	chr4:171641389-171641390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs13114948	chr4:171641420-171641421	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs549975637	chr4:171641423-171641424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78458875	chr4:171641424-171641425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538796081	chr4:171641434-171641435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553610678	chr4:171641435-171641436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571763809	chr4:171641453-171641454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535857345	chr4:171641456-171641457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs140651677	chr4:171641467-171641468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574020224	chr4:171641477-171641478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371428248	chr4:171641510-171641511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs28702559	chr4:171641539-171641540	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs55675109	chr4:171641543-171641544	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs371033669	chr4:171641560-171641561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs578125404	chr4:171641597-171641598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182367543	chr4:171641603-171641604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Neuroblastoma	16790693	CNVD
Developmental delay	22127048	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:171640200-171641200	Enhancers	Fetal Kidney	kidney
2	chr4:171641200-171650000	Weak transcription	Fetal Kidney	kidney
3	chr4:171641800-171642000	Active TSS	Primary B cells from cord blood	blood
4	chr4:171642000-171649200	Weak transcription	Primary B cells from cord blood	blood
5	chr4:171649200-171649800	Enhancers	Primary B cells from cord blood	blood
6	chr4:171649600-171651200	Enhancers	GM12878-XiMat	blood
7	chr4:171650000-171650800	Enhancers	Fetal Kidney	kidney
8	chr4:171657400-171657800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:171657600-171658400	Enhancers	NHEK	skin
10	chr4:171657600-171658600	Enhancers	HMEC	breast
11	chr4:171658600-171661600	Weak transcription	HMEC	breast
12	chr4:171659200-171663000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr4:171660000-171660200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr4:171661600-171662000	Enhancers	HMEC	breast
15	chr4:171662000-171663000	Weak transcription	HMEC	breast
16	chr4:171662600-171663400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr4:171663000-171663400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr4:171663000-171663600	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr4:171663000-171663600	Enhancers	HMEC	breast
20	chr4:171663000-171664600	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr4:171663200-171664200	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr4:171663400-171663600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr4:171663400-171663800	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr4:171663400-171664200	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr4:171663400-171664200	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr4:171663600-171664600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr4:171664600-171665000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr4:171671600-171672000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr4:171691200-171691400	Enhancers	Placenta Amnion	Placenta Amnion
30	chr4:171691400-171692800	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr4:171692800-171694200	Enhancers	Placenta Amnion	Placenta Amnion
32	chr4:171696800-171697000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr4:171697600-171698400	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr4:171698200-171698400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr4:171698200-171698600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr4:171698200-171698600	Enhancers	GM12878-XiMat	blood
37	chr4:171709400-171709600	Enhancers	H1 Cell Line	embryonic stem cell
38	chr4:171709600-171710000	Active TSS	H1 Cell Line	embryonic stem cell
39	chr4:171709600-171710200	Active TSS	H9 Cell Line	embryonic stem cell
40	chr4:171709600-171710200	Active TSS	HUES48 Cell Line	embryonic stem cell
41	chr4:171709600-171710200	Active TSS	HUES64 Cell Line	embryonic stem cell
42	chr4:171709600-171710200	Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr4:171709600-171710400	Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr4:171709800-171710200	Active TSS	iPS-18 Cell Line	embryonic stem cell
45	chr4:171710000-171710200	Enhancers	H1 Cell Line	embryonic stem cell
46	chr4:171726200-171726400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr4:171736800-171737600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
48	chr4:171741200-171744000	Weak transcription	Stomach Mucosa	stomach
49	chr4:171744400-171748400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr4:171748200-171749200	Enhancers	HMEC	breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links