Variant report

Variant	nsv1038384
Chromosome Location	chr14:45447187-45521583
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	ARID3A	chr14:45513907-45514130	HepG2	liver:	n/a	n/a
2	BATF	chr14:45497390-45497737	GM12878	blood:	n/a	n/a
3	BATF	chr14:45497424-45497708	GM12878	blood:	n/a	n/a
4	BCL11A	chr14:45497434-45497723	GM12878	blood:	n/a	n/a
5	BCL11A	chr14:45497556-45497752	GM12878	blood:	n/a	n/a
6	BHLHE40	chr14:45513856-45514183	HepG2	liver:	n/a	n/a
7	BRCA1	chr14:45451804-45451915	H1-hESC	embryonic stem cell:	n/a	n/a
8	CBX3	chr14:45507921-45508531	K562	blood:	n/a	n/a
9	CBX3	chr14:45508113-45508347	K562	blood:	n/a	n/a
10	CEBPB	chr14:45483061-45483432	IMR90	lung:	n/a	chr14:45483236-45483245 chr14:45483236-45483245 chr14:45483236-45483245
11	CEBPB	chr14:45511331-45511427	HepG2	liver:	n/a	n/a
12	CEBPB	chr14:45479105-45479502	HepG2	liver:	n/a	chr14:45479348-45479359 chr14:45479346-45479359 chr14:45479346-45479357 chr14:45479346-45479359 chr14:45479346-45479359
13	CEBPB	chr14:45454182-45454395	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr14:45513955-45514245	HepG2	liver:	n/a	chr14:45514117-45514130 chr14:45514118-45514129
15	CEBPB	chr14:45479014-45479582	K562	blood:	n/a	chr14:45479348-45479359 chr14:45479346-45479359 chr14:45479346-45479357 chr14:45479346-45479359 chr14:45479346-45479359
16	CEBPB	chr14:45479081-45479488	IMR90	lung:	n/a	chr14:45479348-45479359 chr14:45479346-45479359 chr14:45479346-45479357 chr14:45479346-45479359 chr14:45479346-45479359
17	CEBPB	chr14:45482786-45483430	A549	lung:	n/a	chr14:45483236-45483245 chr14:45483236-45483245 chr14:45483236-45483245
18	CEBPB	chr14:45515469-45515722	A549	lung:	n/a	n/a
19	CEBPB	chr14:45483050-45483436	K562	blood:	n/a	chr14:45483236-45483245 chr14:45483236-45483245 chr14:45483236-45483245
20	CEBPB	chr14:45483048-45483351	A549	lung:	n/a	chr14:45483236-45483245 chr14:45483236-45483245 chr14:45483236-45483245
21	CEBPB	chr14:45454864-45454996	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr14:45479190-45479426	H1-hESC	embryonic stem cell:	n/a	chr14:45479348-45479359 chr14:45479346-45479359 chr14:45479346-45479357 chr14:45479346-45479359 chr14:45479346-45479359
23	CEBPB	chr14:45479096-45479472	A549	lung:	n/a	chr14:45479348-45479359 chr14:45479346-45479359 chr14:45479346-45479357 chr14:45479346-45479359 chr14:45479346-45479359
24	CEBPB	chr14:45515502-45515661	K562	blood:	n/a	n/a
25	CEBPB	chr14:45515444-45515747	IMR90	lung:	n/a	n/a
26	CEBPB	chr14:45515512-45515656	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr14:45513948-45514128	A549	lung:	n/a	n/a
28	CEBPB	chr14:45496526-45497009	HepG2	liver:	n/a	chr14:45496640-45496651
29	CEBPB	chr14:45483044-45483461	H1-hESC	embryonic stem cell:	n/a	chr14:45483236-45483245 chr14:45483236-45483245 chr14:45483236-45483245
30	CEBPB	chr14:45483046-45483503	Hela-S3	cervix:	n/a	chr14:45483236-45483245 chr14:45483236-45483245 chr14:45483236-45483245
31	CEBPB	chr14:45482912-45483336	A549	lung:	n/a	chr14:45483236-45483245 chr14:45483236-45483245 chr14:45483236-45483245
32	CEBPB	chr14:45483062-45483417	HepG2	liver:	n/a	chr14:45483236-45483245 chr14:45483236-45483245 chr14:45483236-45483245
33	CTCF	chr14:45451000-45451150	BE2_C	brain:	n/a	n/a
34	CTCF	chr14:45447717-45447785	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr14:45496951-45497001	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr14:45490461-45490561	GM20000	blood:	n/a	n/a
37	CTCF	chr14:45451087-45451170	MCF-7	breast:	n/a	n/a
38	CTCF	chr14:45508522-45508558	GM13976	blood:	n/a	n/a
39	CTCF	chr14:45451116-45451155	MCF-7	breast:	n/a	n/a
40	CUX1	chr14:45451590-45451684	GM12878	blood:	n/a	n/a
41	E2F4	chr14:45455204-45455381	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr14:45484720-45484791	MCF10A-Er-Src	breast:	n/a	chr14:45484721-45484730
43	EBF1	chr14:45459031-45459311	GM12878	blood:	n/a	chr14:45459193-45459204
44	EBF1	chr14:45450547-45450804	GM12878	blood:	n/a	n/a
45	EBF1	chr14:45459173-45459178	GM12878	blood:	n/a	n/a
46	EBF1	chr14:45459040-45459301	GM12878	blood:	n/a	chr14:45459193-45459204
47	EBF1	chr14:45497490-45497767	GM12878	blood:	n/a	n/a
48	EP300	chr14:45465069-45465493	A549	lung:	n/a	chr14:45465173-45465182 chr14:45465174-45465183
49	ESR1	chr14:45448889-45449091	T-47D	breast:	n/a	n/a
50	ESR1	chr14:45448881-45449231	T-47D	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:45447939..45449811-chr14:45461591..45463970,2	MCF-7	breast:
2	chr14:45429271..45433674-chr14:45463003..45467131,6	MCF-7	breast:
3	chr14:45510248..45513228-chr14:45553059..45554634,2	MCF-7	breast:
4	chr14:45513966..45516650-chr14:45524638..45526373,2	MCF-7	breast:
5	chr14:45427812..45430166-chr14:45450519..45452752,2	MCF-7	breast:
6	chr14:45447939..45449811-chr14:45461591..45463970,2	MCF-7	breast:
7	chr14:45431180..45433416-chr14:45447895..45450049,3	MCF-7	breast:
8	chr14:45442937..45446932-chr14:45447950..45450960,3	MCF-7	breast:
9	chr14:45500095..45501795-chr17:41400297..41401961,2	MCF-7	breast:
10	chr14:45437222..45438857-chr14:45461418..45463222,2	MCF-7	breast:
11	chr14:45461379..45464439-chr14:45465878..45468676,3	MCF-7	breast:
12	chr14:45478064..45480490-chr14:45481016..45483752,3	K562	blood:
13	chr14:45382331..45385097-chr14:45486659..45488651,2	MCF-7	breast:
14	chr14:45461379..45464439-chr14:45465878..45468676,3	MCF-7	breast:
15	chr14:45430257..45433582-chr14:45504666..45507848,3	MCF-7	breast:
16	chr14:45471186..45473239-chr14:45488611..45490620,2	K562	blood:
17	chr14:45501888..45504415-chr14:45528561..45531517,2	MCF-7	breast:
18	chr14:45429455..45434456-chr14:45457577..45465953,9	MCF-7	breast:
19	chr14:45430346..45432834-chr14:45446058..45448249,2	MCF-7	breast:
20	chr14:45516713..45518347-chr14:45551728..45554055,3	MCF-7	breast:
21	chr14:45432779..45434655-chr14:45476453..45478128,2	MCF-7	breast:
22	chr14:45471186..45473239-chr14:45488611..45490620,2	K562	blood:
23	chr14:45430922..45432847-chr14:45466321..45468139,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRPF39-2	chr14:45497379-45497499	NONHSAT036630
2	lnc-PRPF39-2	chr14:45481090-45481278	NONHSAT036630
3	lnc-PRPF39-2	chr14:45494676-45495075	NONHSAT036631
4	lnc-PRPF39-2	chr14:45494986-45495075	NONHSAT036630
5	lnc-PRPF39-2	chr14:45496502-45496677	NONHSAT036630
6	lnc-PRPF39-2	chr14:45496502-45496537	NONHSAT036631

Variant related genes	Relation type
FAM179B	TF binding region
KLHL28	TF binding region
ENSG00000185246	chromatin interactions
ENSG00000198718	chromatin interactions
ENSG00000249163	chromatin interactions
ENSG00000179454	chromatin interactions

Extended variants
information (count: 2582 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2582 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11846656	chr14:45447187-45447188	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558375364	chr14:45447188-45447189	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs566608611	chr14:45447240-45447241	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs145536288	chr14:45447245-45447246	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs73350114	chr14:45447254-45447255	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs562180774	chr14:45447318-45447319	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs184411921	chr14:45447379-45447380	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs541744827	chr14:45447414-45447415	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs560361251	chr14:45447545-45447546	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs147289430	chr14:45447597-45447598	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs11846891	chr14:45447707-45447708	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs564122608	chr14:45447728-45447729	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs10136855	chr14:45447759-45447760	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs10136926	chr14:45447781-45447782	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs569300929	chr14:45447881-45447882	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs151276572	chr14:45447967-45447968	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs140441001	chr14:45447985-45447986	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs112270973	chr14:45448021-45448022	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs374904076	chr14:45448029-45448030	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs567110790	chr14:45448039-45448040	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs549039998	chr14:45448043-45448044	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs534130687	chr14:45448047-45448048	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs559148892	chr14:45448068-45448069	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs4321108	chr14:45448084-45448085	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs577009111	chr14:45448091-45448092	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs537579968	chr14:45448094-45448095	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs149995293	chr14:45448126-45448127	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs568855897	chr14:45448175-45448176	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs574110751	chr14:45448180-45448181	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs531667129	chr14:45448190-45448191	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs201855402	chr14:45448235-45448236	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs79983664	chr14:45448270-45448271	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs572351733	chr14:45448273-45448274	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs188800183	chr14:45448343-45448344	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs144833686	chr14:45448375-45448376	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs367900085	chr14:45448376-45448377	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs201212449	chr14:45448395-45448396	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs10140049	chr14:45448398-45448399	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs564338768	chr14:45448454-45448455	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs531510931	chr14:45448460-45448461	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs551115380	chr14:45448491-45448492	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs562933121	chr14:45448521-45448522	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs10139998	chr14:45448564-45448565	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs536733150	chr14:45448578-45448579	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs192024049	chr14:45448642-45448643	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs145606315	chr14:45448672-45448673	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs534547117	chr14:45448757-45448758	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs556164744	chr14:45448788-45448789	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs552574627	chr14:45448857-45448858	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs377100144	chr14:45449119-45449120	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:1583 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:45434600-45465000	Weak transcription	Fetal Thymus	thymus
2	chr14:45436200-45486600	Weak transcription	Gastric	stomach
3	chr14:45436800-45461400	Weak transcription	K562	blood
4	chr14:45437000-45449000	Weak transcription	Fetal Stomach	stomach
5	chr14:45437000-45451800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr14:45437000-45465000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr14:45437000-45465800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr14:45437000-45473200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr14:45437000-45496000	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr14:45437000-45507400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr14:45437000-45514600	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr14:45437200-45449400	Weak transcription	Liver	Liver
13	chr14:45437200-45466000	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr14:45437200-45469400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr14:45438000-45501800	Weak transcription	Fetal Kidney	kidney
16	chr14:45438200-45448600	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr14:45438200-45449000	Weak transcription	Adipose Nuclei	Adipose
18	chr14:45438200-45465400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr14:45438600-45448400	Weak transcription	Fetal Intestine Large	intestine
20	chr14:45438600-45451800	Weak transcription	Brain Cingulate Gyrus	brain
21	chr14:45438800-45447800	Weak transcription	Fetal Intestine Small	intestine
22	chr14:45438800-45449600	Weak transcription	Left Ventricle	heart
23	chr14:45439200-45448400	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr14:45439200-45464400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr14:45439400-45448400	Weak transcription	Psoas Muscle	Psoas
26	chr14:45439400-45449000	Weak transcription	Brain Angular Gyrus	brain
27	chr14:45440000-45465400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr14:45440400-45465800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr14:45441400-45448800	Weak transcription	Primary B cells from cord blood	blood
30	chr14:45441400-45449200	Weak transcription	Fetal Lung	lung
31	chr14:45441400-45469400	Weak transcription	Primary T cells from cord blood	blood
32	chr14:45442200-45458000	Weak transcription	Primary hematopoietic stem cells	blood
33	chr14:45442800-45457800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr14:45443400-45448600	Weak transcription	Brain Anterior Caudate	brain
35	chr14:45444000-45448800	Weak transcription	Fetal Muscle Leg	muscle
36	chr14:45444000-45451400	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr14:45444200-45448400	Weak transcription	Hela-S3	cervix
38	chr14:45444200-45448600	Weak transcription	Fetal Heart	heart
39	chr14:45444400-45452000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr14:45444400-45452400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr14:45444600-45451800	Weak transcription	GM12878-XiMat	blood
42	chr14:45445600-45448800	Weak transcription	Brain Substantia Nigra	brain
43	chr14:45445800-45448400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr14:45447400-45447600	Enhancers	Duodenum Smooth Muscle	Duodenum
45	chr14:45447600-45449400	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr14:45447800-45448600	Weak transcription	Fetal Brain Female	brain
47	chr14:45447800-45448600	Strong transcription	Fetal Intestine Small	intestine
48	chr14:45448400-45449200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr14:45448400-45449200	Strong transcription	Fetal Intestine Large	intestine
50	chr14:45448400-45449800	Enhancers	Brain Inferior Temporal Lobe	brain

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