Variant report

Variant	nsv878690
Chromosome Location	chr4:9944650-10008305
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:715)
CpG islands
(count:244)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:715 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:9952887-9953127	K562	blood:	n/a	n/a
2	ARID3A	chr4:10007887-10008235	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:10004013-10004296	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:9998163-9998719	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:9965207-9965232	HepG2	liver:	n/a	n/a
6	ATF2	chr4:10001424-10002312	GM12878	blood:	n/a	n/a
7	ATF2	chr4:9991905-9992354	GM12878	blood:	n/a	n/a
8	ATF2	chr4:10005306-10005725	GM12878	blood:	n/a	n/a
9	ATF2	chr4:9972118-9972587	GM12878	blood:	n/a	n/a
10	ATF2	chr4:10001436-10002278	GM12878	blood:	n/a	n/a
11	ATF2	chr4:10007760-10008278	GM12878	blood:	n/a	n/a
12	ATF2	chr4:10007851-10008196	GM12878	blood:	n/a	n/a
13	ATF3	chr4:10003452-10003631	K562	blood:	n/a	n/a
14	BATF	chr4:10005411-10005658	GM12878	blood:	n/a	chr4:10005512-10005523
15	BATF	chr4:9972302-9972703	GM12878	blood:	n/a	n/a
16	BATF	chr4:10001742-10002251	GM12878	blood:	n/a	n/a
17	BCL11A	chr4:9972312-9972693	GM12878	blood:	n/a	n/a
18	BCL11A	chr4:9972269-9972776	GM12878	blood:	n/a	n/a
19	BCL3	chr4:10007752-10008155	GM12878	blood:	n/a	n/a
20	BCL3	chr4:9991562-9991944	GM12878	blood:	n/a	n/a
21	BCL3	chr4:9989936-9990316	GM12878	blood:	n/a	n/a
22	BCL3	chr4:10005262-10005711	GM12878	blood:	n/a	n/a
23	BCL3	chr4:9989903-9990331	GM12878	blood:	n/a	n/a
24	BCL3	chr4:9991620-9991908	GM12878	blood:	n/a	n/a
25	BCLAF1	chr4:9972208-9972590	GM12878	blood:	n/a	n/a
26	BCLAF1	chr4:10007701-10008311	GM12878	blood:	n/a	n/a
27	BHLHE40	chr4:10003903-10004201	GM12878	blood:	n/a	n/a
28	BHLHE40	chr4:9964308-9964572	GM12878	blood:	n/a	n/a
29	BHLHE40	chr4:9972158-9972605	GM12878	blood:	n/a	n/a
30	BHLHE40	chr4:9962047-9962396	GM12878	blood:	n/a	n/a
31	BHLHE40	chr4:10007886-10008835	HepG2	liver:	n/a	n/a
32	BHLHE40	chr4:9983862-9984078	K562	blood:	n/a	n/a
33	BHLHE40	chr4:10007812-10009749	GM12878	blood:	n/a	n/a
34	BRCA1	chr4:10008036-10008235	HepG2	liver:	n/a	n/a
35	BRCA1	chr4:9987308-9987348	GM12878	blood:	n/a	n/a
36	CEBPB	chr4:9954023-9954436	MCF-7	breast:	n/a	chr4:9954213-9954224
37	CEBPB	chr4:10007707-10008323	A549	lung:	n/a	n/a
38	CEBPB	chr4:9954068-9954391	HepG2	liver:	n/a	chr4:9954213-9954224
39	CEBPB	chr4:9954044-9954358	K562	blood:	n/a	chr4:9954213-9954224
40	CEBPB	chr4:9954066-9954414	HepG2	liver:	n/a	chr4:9954213-9954224
41	CEBPB	chr4:10007846-10008230	A549	lung:	n/a	n/a
42	CEBPB	chr4:10007852-10008196	HepG2	liver:	n/a	n/a
43	CEBPB	chr4:9954137-9954295	HepG2	liver:	n/a	chr4:9954213-9954224
44	CEBPB	chr4:10007804-10008320	MCF-7	breast:	n/a	n/a
45	CEBPB	chr4:10007842-10008822	HepG2	liver:	n/a	n/a
46	CEBPB	chr4:10007703-10008326	MCF-7	breast:	n/a	n/a
47	CEBPB	chr4:10007797-10008276	ECC-1	luminal epithelium:	n/a	n/a
48	CEBPB	chr4:10007870-10008188	ECC-1	luminal epithelium:	n/a	n/a
49	CEBPB	chr4:9954030-9954437	MCF-7	breast:	n/a	chr4:9954213-9954224
50	CEBPB	chr4:9954171-9954281	K562	blood:	n/a	chr4:9954213-9954224

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9981202-9981252	HPAEpiC	pulmonary alveolar:	n/a
2	chr4:9950643-9950693	AG10803	skin:	n/a
3	chr4:9998017-9998067	BE2_C	brain:	n/a
4	chr4:9990048-9990098	HCF	heart:	n/a
5	chr4:9950643-9950693	HRPEpiC	eye:	n/a
6	chr4:9981202-9981252	Hepatocyte	liver:	n/a
7	chr4:9950643-9950693	LNCaP	prostate:	n/a
8	chr4:9950643-9950693	AG09319	gingival:	n/a
9	chr4:9981202-9981252	MCF-7	breast:	n/a
10	chr4:9998017-9998067	HCF	heart:	n/a
11	chr4:9950643-9950693	PrEC	prostate:	n/a
12	chr4:9981202-9981252	HEEpiC	esophagus:	n/a
13	chr4:9990048-9990098	Caco-2	colon:	n/a
14	chr4:9950643-9950693	NHDF-neo	bronchial:	n/a
15	chr4:9990048-9990098	NH-A	brain:	n/a
16	chr4:9990048-9990098	Jurkat	blood:	n/a
17	chr4:9990048-9990098	AG09319	gingival:	n/a
18	chr4:9950643-9950693	HEK293	kidney:	embryo
19	chr4:9998017-9998067	NHBE	bronchial:	n/a
20	chr4:9950643-9950693	AoSMC	blood vessel:	n/a
21	chr4:9981202-9981252	ECC-1	luminal epithelium:	n/a
22	chr4:9998017-9998067	HIPEpiC	eye:	n/a
23	chr4:9990048-9990098	GM12878	blood:	n/a
24	chr4:9950643-9950693	U87	brain:	n/a
25	chr4:9981202-9981252	K562	blood:	n/a
26	chr4:9981202-9981252	NHBE	bronchial:	n/a
27	chr4:9950643-9950693	HepG2	liver:	n/a
28	chr4:9950643-9950693	HNPCEpiC	eye:	n/a
29	chr4:9990048-9990098	AG04449	skin:	fetal
30	chr4:9981202-9981252	HCF	heart:	n/a
31	chr4:9981202-9981252	AoSMC	blood vessel:	n/a
32	chr4:9990048-9990098	Hepatocyte	liver:	n/a
33	chr4:9990048-9990098	PANC-1	pancreas:	n/a
34	chr4:9990048-9990098	HCPEpiC	choroid plexus:	n/a
35	chr4:9981202-9981252	HUVEC	blood vessel:	n/a
36	chr4:9950643-9950693	PANC-1	pancreas:	n/a
37	chr4:9990048-9990098	GM06990	blood:	n/a
38	chr4:9998017-9998067	MCF-7	breast:	n/a
39	chr4:9998017-9998067	HCT-116	colon:	n/a
40	chr4:9998017-9998067	HRE	kidney:	n/a
41	chr4:9998017-9998067	AG04449	skin:	fetal
42	chr4:9950643-9950693	GM19239	blood:	n/a
43	chr4:9998017-9998067	HepG2	liver:	n/a
44	chr4:9981202-9981252	GM06990	blood:	n/a
45	chr4:9950643-9950693	ECC-1	luminal epithelium:	n/a
46	chr4:9998017-9998067	AG04450	lung:	fetal
47	chr4:9981202-9981252	H1-hESC	embryonic stem cell:	embryo
48	chr4:9950643-9950693	K562	blood:	n/a
49	chr4:9950643-9950693	HEEpiC	esophagus:	n/a
50	chr4:9998017-9998067	SK-N-MC	brain:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:9957351..9959521-chr4:10008550..10011275,2	MCF-7	breast:
2	chr4:9999663..10002309-chr4:10003898..10006601,3	MCF-7	breast:
3	chr4:9999663..10002309-chr4:10003898..10006601,3	MCF-7	breast:
4	chr4:9959731..9961810-chr4:9971031..9973164,2	K562	blood:
5	chr4:9959731..9961810-chr4:9971031..9973164,2	K562	blood:
6	chr4:9924672..9926796-chr4:10008145..10009788,2	MCF-7	breast:
7	chr4:9999925..10002392-chr4:10005670..10008448,2	K562	blood:
8	chr4:10003454..10005588-chr4:10009688..10011673,2	MCF-7	breast:
9	chr4:9761130..9763005-chr4:9988480..9990175,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DRD5-2	chr4:10008106-10008316	ENSG00000250413.1

No data

Variant related genes	Relation type
ENSG00000250413	TF binding region
ENSG00000250413	CpG island
ENSG00000250413	chromatin interactions

Extended variants
information (count: 2957 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2957 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6449144	chr4:9944650-9944651	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs376973862	chr4:9944701-9944702	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs550458406	chr4:9944713-9944714	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147107006	chr4:9944724-9944725	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs182592473	chr4:9944765-9944766	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547701296	chr4:9944779-9944780	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs543120762	chr4:9944828-9944829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565750161	chr4:9944829-9944830	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs535932112	chr4:9944842-9944843	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558655181	chr4:9944895-9944896	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554670875	chr4:9944900-9944901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138558177	chr4:9944956-9944957	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186419953	chr4:9944989-9944990	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558427212	chr4:9945011-9945012	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190683606	chr4:9945013-9945014	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181452327	chr4:9945038-9945039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552859847	chr4:9945084-9945085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115768657	chr4:9945085-9945086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542710155	chr4:9945092-9945093	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561446728	chr4:9945096-9945097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531731568	chr4:9945103-9945104	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543881674	chr4:9945114-9945115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs1007872	chr4:9945148-9945149	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs371199910	chr4:9945216-9945217	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185792204	chr4:9945221-9945222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs190373872	chr4:9945222-9945223	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377690697	chr4:9945249-9945250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112484309	chr4:9945251-9945252	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143239812	chr4:9945278-9945279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4235346	chr4:9945296-9945297	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs569459020	chr4:9945322-9945323	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148311631	chr4:9945352-9945353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141464777	chr4:9945355-9945356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570129905	chr4:9945404-9945405	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542155945	chr4:9945469-9945470	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs534588079	chr4:9945472-9945473	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs553237280	chr4:9945476-9945477	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs376788101	chr4:9945478-9945479	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs116484962	chr4:9945482-9945483	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs146343790	chr4:9945483-9945484	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs370586133	chr4:9945494-9945495	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs555095473	chr4:9945518-9945519	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186261707	chr4:9945526-9945527	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs190733254	chr4:9945536-9945537	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs139285468	chr4:9945546-9945547	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs577330763	chr4:9945595-9945596	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs374619261	chr4:9945647-9945648	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs184088622	chr4:9945651-9945652	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs116012279	chr4:9945652-9945653	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs530221790	chr4:9945680-9945681	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	17142309	CNVD
Schizophrenia	23813976	CNVD
Glioma	20126413	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:806 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9911400-9979800	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr4:9918600-9948600	Weak transcription	Pancreas	Pancrea
3	chr4:9926400-9951600	Weak transcription	Spleen	Spleen
4	chr4:9926800-9948000	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr4:9927000-9948600	Weak transcription	Right Ventricle	heart
6	chr4:9927800-9948400	Strong transcription	HepG2	liver
7	chr4:9928000-9960000	Weak transcription	Esophagus	oesophagus
8	chr4:9929600-9948600	Weak transcription	Left Ventricle	heart
9	chr4:9930600-9946200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr4:9930800-9952200	Strong transcription	Primary monocytes fromperipheralblood	blood
11	chr4:9930800-9953800	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr4:9931000-9946600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr4:9933600-9951200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr4:9937000-9945800	Strong transcription	Fetal Intestine Small	intestine
15	chr4:9938200-9957600	Weak transcription	Fetal Stomach	stomach
16	chr4:9939600-9956600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr4:9941000-9948800	Weak transcription	Liver	Liver
18	chr4:9941400-9953200	Weak transcription	Stomach Smooth Muscle	stomach
19	chr4:9942000-9949400	Weak transcription	Ovary	ovary
20	chr4:9942200-9948800	Weak transcription	Gastric	stomach
21	chr4:9942600-9945400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr4:9944000-9946600	Weak transcription	NHEK	skin
23	chr4:9944000-9979400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr4:9944400-9948600	Weak transcription	Duodenum Mucosa	Duodenum
25	chr4:9944600-9944800	Enhancers	Lung	lung
26	chr4:9944600-9944800	Enhancers	Placenta Amnion	Placenta Amnion
27	chr4:9944600-9946600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr4:9944600-9947200	Weak transcription	Fetal Intestine Large	intestine
29	chr4:9944600-9964400	Weak transcription	HMEC	breast
30	chr4:9944800-9945600	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr4:9945400-9945600	Enhancers	Fetal Muscle Trunk	muscle
32	chr4:9945400-9945800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr4:9945400-9947000	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr4:9945600-9947800	Enhancers	Placenta Amnion	Placenta Amnion
35	chr4:9945600-9949200	Weak transcription	Fetal Muscle Trunk	muscle
36	chr4:9945800-9946000	Genic enhancers	Fetal Intestine Small	intestine
37	chr4:9946000-9946600	Weak transcription	Fetal Intestine Small	intestine
38	chr4:9946200-9948000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr4:9946200-9948800	Weak transcription	Psoas Muscle	Psoas
40	chr4:9946600-9947000	Enhancers	Fetal Intestine Small	intestine
41	chr4:9946600-9947000	Enhancers	Stomach Mucosa	stomach
42	chr4:9946600-9947000	Genic enhancers	NHEK	skin
43	chr4:9946600-9947400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr4:9946600-9947400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr4:9947000-9947200	Weak transcription	Fetal Intestine Small	intestine
46	chr4:9947000-9947400	Enhancers	NHEK	skin
47	chr4:9947000-9948400	Weak transcription	Stomach Mucosa	stomach
48	chr4:9947200-9947600	Strong transcription	Fetal Intestine Large	intestine
49	chr4:9947200-9947800	Strong transcription	Fetal Intestine Small	intestine
50	chr4:9947400-9947800	Weak transcription	NHEK	skin

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