Variant report

Variant	nsv916423
Chromosome Location	chr16:59411801-59750824
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	chr16:59552701-59552977	K562	blood:	n/a	n/a
2	ATF1	chr16:59574603-59574647	K562	blood:	n/a	n/a
3	ATF1	chr16:59512519-59513106	K562	blood:	n/a	n/a
4	ATF1	chr16:59418654-59418858	K562	blood:	n/a	n/a
5	ATF3	chr16:59607286-59608197	A549	lung:	n/a	chr16:59607669-59607680 chr16:59607669-59607680 chr16:59607671-59607679 chr16:59607669-59607682
6	ATF3	chr16:59607268-59608238	A549	lung:	n/a	chr16:59607669-59607680 chr16:59607669-59607680 chr16:59607671-59607679 chr16:59607669-59607682
7	BACH1	chr16:59459499-59459576	K562	blood:	n/a	n/a
8	BACH1	chr16:59637252-59637310	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL3	chr16:59561024-59561679	A549	lung:	n/a	n/a
10	BCL3	chr16:59607250-59608289	A549	lung:	n/a	chr16:59607950-59607959
11	BCL3	chr16:59607280-59608220	A549	lung:	n/a	chr16:59607950-59607959
12	CEBPB	chr16:59731195-59731541	IMR90	lung:	n/a	n/a
13	CEBPB	chr16:59638167-59638644	A549	lung:	n/a	chr16:59638376-59638387 chr16:59638376-59638389 chr16:59638185-59638197 chr16:59638376-59638387 chr16:59638377-59638388
14	CEBPB	chr16:59728966-59729119	K562	blood:	n/a	chr16:59729056-59729067
15	CEBPB	chr16:59639781-59639958	K562	blood:	n/a	chr16:59639806-59639817
16	CEBPB	chr16:59641136-59641336	A549	lung:	n/a	n/a
17	CEBPB	chr16:59611123-59611379	HepG2	liver:	n/a	chr16:59611239-59611250
18	CEBPB	chr16:59607305-59607809	A549	lung:	n/a	chr16:59607756-59607768
19	CEBPB	chr16:59667835-59668479	IMR90	lung:	n/a	n/a
20	CEBPB	chr16:59436345-59436609	HepG2	liver:	n/a	chr16:59436471-59436484 chr16:59436473-59436482 chr16:59436473-59436482 chr16:59436473-59436482 chr16:59436473-59436484 chr16:59436471-59436484 chr16:59436473-59436482 chr16:59436471-59436482
21	CEBPB	chr16:59639640-59639961	HepG2	liver:	n/a	chr16:59639776-59639787 chr16:59639806-59639817
22	CEBPB	chr16:59607195-59608611	A549	lung:	n/a	chr16:59608246-59608258 chr16:59607756-59607768
23	CEBPB	chr16:59699676-59699852	A549	lung:	n/a	chr16:59699727-59699740 chr16:59699728-59699739 chr16:59699729-59699738
24	CEBPB	chr16:59627070-59627695	IMR90	lung:	n/a	chr16:59627251-59627264
25	CEBPB	chr16:59440743-59440844	IMR90	lung:	n/a	chr16:59440793-59440804
26	CEBPB	chr16:59674581-59674822	A549	lung:	n/a	chr16:59674679-59674690 chr16:59674668-59674679
27	CEBPB	chr16:59717805-59717880	A549	lung:	n/a	n/a
28	CEBPB	chr16:59607352-59608186	IMR90	lung:	n/a	chr16:59607756-59607768
29	CEBPB	chr16:59728926-59729209	A549	lung:	n/a	chr16:59729056-59729067
30	CEBPB	chr16:59732911-59733165	HepG2	liver:	n/a	n/a
31	CEBPB	chr16:59503917-59504195	IMR90	lung:	n/a	chr16:59504092-59504105 chr16:59504092-59504105 chr16:59504092-59504105 chr16:59504092-59504103 chr16:59504094-59504105
32	CEBPB	chr16:59419976-59420242	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr16:59702500-59702739	IMR90	lung:	n/a	chr16:59702597-59702608
34	CEBPB	chr16:59639635-59639988	IMR90	lung:	n/a	chr16:59639776-59639787 chr16:59639806-59639817
35	CEBPB	chr16:59509576-59509726	HepG2	liver:	n/a	chr16:59509680-59509691
36	CEBPB	chr16:59639646-59640003	A549	lung:	n/a	chr16:59639776-59639787 chr16:59639806-59639817
37	CEBPB	chr16:59728890-59729203	IMR90	lung:	n/a	chr16:59729056-59729067
38	CEBPB	chr16:59607369-59608128	A549	lung:	n/a	chr16:59607756-59607768
39	CEBPB	chr16:59702527-59702671	HepG2	liver:	n/a	chr16:59702597-59702608
40	CEBPB	chr16:59672961-59673060	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr16:59619057-59619288	HepG2	liver:	n/a	n/a
42	CEBPB	chr16:59699560-59699871	IMR90	lung:	n/a	chr16:59699727-59699740 chr16:59699728-59699739 chr16:59699729-59699738
43	CEBPB	chr16:59473388-59473652	HepG2	liver:	n/a	chr16:59473555-59473566
44	CEBPB	chr16:59606859-59607041	A549	lung:	n/a	n/a
45	CEBPB	chr16:59607451-59607761	HepG2	liver:	n/a	n/a
46	CEBPB	chr16:59547514-59547710	A549	lung:	n/a	n/a
47	CEBPB	chr16:59652494-59652790	HepG2	liver:	n/a	chr16:59652665-59652676
48	CEBPB	chr16:59558827-59559042	A549	lung:	n/a	chr16:59558913-59558924 chr16:59558913-59558926 chr16:59558913-59558926 chr16:59558914-59558925 chr16:59558913-59558926
49	CEBPB	chr16:59445863-59446338	A549	lung:	n/a	chr16:59446020-59446033
50	CEBPB	chr16:59558777-59559010	K562	blood:	n/a	chr16:59558913-59558924 chr16:59558913-59558926 chr16:59558913-59558926 chr16:59558914-59558925 chr16:59558913-59558926

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:59602460-59602510	AoSMC	blood vessel:	n/a
2	chr16:59656293-59656343	HRE	kidney:	n/a
3	chr16:59602460-59602510	HEEpiC	esophagus:	n/a
4	chr16:59656293-59656343	A549	lung:	n/a
5	chr16:59627519-59627569	SK-N-SH_RA	brain:	n/a
6	chr16:59602460-59602510	ovcar-3	ovarian:	n/a
7	chr16:59602460-59602510	A549	lung:	n/a
8	chr16:59602460-59602510	NH-A	brain:	n/a
9	chr16:59627519-59627569	HIPEpiC	eye:	n/a
10	chr16:59656293-59656343	SAEC	small airway:	n/a
11	chr16:59602460-59602510	GM12892	blood:	n/a
12	chr16:59656293-59656343	K562	blood:	n/a
13	chr16:59627519-59627569	HEEpiC	esophagus:	n/a
14	chr16:59656293-59656343	NT2-D1	testis:	n/a
15	chr16:59602460-59602510	K562	blood:	n/a
16	chr16:59602460-59602510	GM12891	blood:	n/a
17	chr16:59602460-59602510	PFSK-1	brain:	n/a
18	chr16:59627519-59627569	NHBE	bronchial:	n/a
19	chr16:59627519-59627569	K562	blood:	n/a
20	chr16:59656293-59656343	HRPEpiC	eye:	n/a
21	chr16:59627519-59627569	LNCaP	prostate:	n/a
22	chr16:59656293-59656343	AG04450	lung:	fetal
23	chr16:59656293-59656343	HMEC	breast:	n/a
24	chr16:59627519-59627569	SK-N-MC	brain:	n/a
25	chr16:59656293-59656343	NH-A	brain:	n/a
26	chr16:59602460-59602510	GM19239	blood:	n/a
27	chr16:59656293-59656343	MCF-7	breast:	n/a
28	chr16:59627519-59627569	A549	lung:	n/a
29	chr16:59602460-59602510	HCF	heart:	n/a
30	chr16:59627519-59627569	NB4	blood:	n/a
31	chr16:59656293-59656343	SK-N-SH	brain:	n/a
32	chr16:59656293-59656343	LNCaP	prostate:	n/a
33	chr16:59656293-59656343	HNPCEpiC	eye:	n/a
34	chr16:59656293-59656343	ECC-1	luminal epithelium:	n/a
35	chr16:59627519-59627569	GM12892	blood:	n/a
36	chr16:59627519-59627569	ovcar-3	ovarian:	n/a
37	chr16:59602460-59602510	HMEC	breast:	n/a
38	chr16:59627519-59627569	AoSMC	blood vessel:	n/a
39	chr16:59627519-59627569	Jurkat	blood:	n/a
40	chr16:59656293-59656343	IMR90	lung:	fetal
41	chr16:59627519-59627569	MCF-7	breast:	n/a
42	chr16:59656293-59656343	HIPEpiC	eye:	n/a
43	chr16:59656293-59656343	AG09309	skin:	n/a
44	chr16:59656293-59656343	HL-60	blood:	n/a
45	chr16:59602460-59602510	U87	brain:	n/a
46	chr16:59627519-59627569	MCF10A-Er-Src	breast:	n/a
47	chr16:59627519-59627569	Hela-S3	cervix:	n/a
48	chr16:59656293-59656343	GM12892	blood:	n/a
49	chr16:59602460-59602510	SK-N-SH_RA	brain:	n/a
50	chr16:59627519-59627569	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:59581382..59583967-chr16:59590690..59593280,2	MCF-7	breast:
2	chr16:59445008..59446636-chr16:59454260..59456592,2	K562	blood:
3	chr16:59519600..59521428-chr16:59529672..59531937,2	K562	blood:
4	chr16:59581382..59583967-chr16:59590690..59593280,2	MCF-7	breast:
5	chr16:59635524..59637585-chr16:59638803..59640976,2	K562	blood:
6	chr16:59730238..59732939-chr3:97563003..97565712,2	MCF-7	breast:
7	chr16:59635524..59637585-chr16:59638803..59640976,2	K562	blood:
8	chr16:59710678..59713121-chr16:59778438..59780009,2	K562	blood:
9	chr16:59445008..59446636-chr16:59454260..59456592,2	K562	blood:
10	chr16:59464240..59466061-chr16:59467687..59469793,2	K562	blood:
11	chr16:59464240..59466061-chr16:59467687..59469793,2	K562	blood:
12	chr16:59519600..59521428-chr16:59529672..59531937,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-105C20.2.1-1	chr16:59497608-59497658	XLOC_011972
2	lnc-RP11-105C20.2.1-2	chr16:59438650-59438797	XLOC_011971
3	lnc-RP11-105C20.2.1-2	chr16:59436484-59436576	XLOC_011971
4	lnc-RP11-105C20.2.1-1	chr16:59475882-59476136	XLOC_011972
5	lnc-RP11-105C20.2.1-5	chr16:59743897-59744027	NONHSAT142892
6	lnc-RP11-105C20.2.1-5	chr16:59744120-59744199	NONHSAT142892
7	lnc-RP11-105C20.2.1-2	chr16:59445379-59445573	XLOC_011971
8	lnc-SETD6-13	chr16:59689506-59689824	NONHSAT142891
9	lnc-SETD6-13	chr16:59690034-59690240	NONHSAT142891

Variant related genes	Relation type
RNU4-58P	TF binding region
ENSG00000238601	TF binding region
ENSG00000270222	TF binding region
RNU4-58P	CpG island
ENSG00000238601	CpG island
ENSG00000270222	CpG island
KIAA1586	miRNA target sites
KIAA1549	miRNA target sites

Extended variants
information (count: 8252 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:8252 , 50 per page) page: 1 2 3 4 5 6 7 ... 166

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564258034	chr16:59413016-59413017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs549524274	chr16:59413046-59413047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571459689	chr16:59413050-59413051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs568053448	chr16:59413082-59413083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs9926716	chr16:59413098-59413099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183402064	chr16:59413110-59413111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs568587410	chr16:59413114-59413115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188475478	chr16:59413118-59413119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192997268	chr16:59413139-59413140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147710579	chr16:59413183-59413184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs202076486	chr16:59413203-59413204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs200499272	chr16:59413205-59413206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539827805	chr16:59413221-59413222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184852567	chr16:59413232-59413233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532301086	chr16:59413237-59413238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs373040438	chr16:59413260-59413261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535327373	chr16:59413368-59413369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs536425568	chr16:59419003-59419004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567723136	chr16:59419015-59419016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554713567	chr16:59419023-59419024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs576341622	chr16:59419034-59419035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543666500	chr16:59419087-59419088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs79393849	chr16:59419116-59419117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs77006938	chr16:59419133-59419134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541551470	chr16:59419138-59419139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs529988898	chr16:59419182-59419183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs559573681	chr16:59419206-59419207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs112752951	chr16:59419223-59419224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs145519487	chr16:59419243-59419244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141333701	chr16:59419301-59419302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs397855478	chr16:59419320-59419321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs549487704	chr16:59419321-59419322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs34990673	chr16:59419322-59419323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs34172895	chr16:59419324-59419325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs142445488	chr16:59419363-59419364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs398029566	chr16:59419365-59419366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs563433983	chr16:59419371-59419372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs530831625	chr16:59419433-59419434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529985628	chr16:59419444-59419445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs16961034	chr16:59419461-59419462	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs570468672	chr16:59419502-59419503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs138985136	chr16:59419606-59419607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546702690	chr16:59419613-59419614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs140716666	chr16:59419636-59419637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs535142702	chr16:59419638-59419639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs180981359	chr16:59419660-59419661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs143834692	chr16:59419688-59419689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs117458399	chr16:59419755-59419756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs558975530	chr16:59419812-59419813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs577199064	chr16:59419830-59419831	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Infertility	21528002	CNVD
Breast cancer	21806811	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Neurodevelopmental disorder	22521361	CNVD
Glioblastoma multiforme	22286061	CNVD
Autism	18414403	CNVD
Breast cancer	20409316	CNVD
Chordoma	18071362	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Ovarian cancer	21720365	CNVD
Leiomyosarcoma	16982739	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	20972252	CNVD
Invasive breast cancer	20972252	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:655 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:59413000-59413400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr16:59419000-59420600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr16:59419200-59419800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr16:59419200-59419800	Enhancers	NHDF-Ad	bronchial
5	chr16:59419200-59420000	Enhancers	HSMM	muscle
6	chr16:59419200-59420000	Enhancers	HSMMtube	muscle
7	chr16:59419200-59420000	Enhancers	NH-A	brain
8	chr16:59419200-59420000	Enhancers	NHLF	lung
9	chr16:59419200-59420200	Enhancers	Fetal Stomach	stomach
10	chr16:59419200-59420400	Enhancers	Fetal Lung	lung
11	chr16:59419200-59420600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr16:59419200-59420600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr16:59419400-59419800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr16:59419400-59420000	Enhancers	Muscle Satellite Cultured Cells	--
15	chr16:59419400-59420000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr16:59419400-59420600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr16:59419600-59420000	Enhancers	Adipose Nuclei	Adipose
18	chr16:59419600-59420200	Enhancers	Duodenum Smooth Muscle	Duodenum
19	chr16:59419600-59420400	Enhancers	Osteobl	bone
20	chr16:59419800-59420200	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr16:59419800-59420200	Enhancers	Fetal Muscle Leg	muscle
22	chr16:59422800-59427200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr16:59423000-59423400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr16:59423400-59425600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr16:59425600-59427200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr16:59425800-59426000	Bivalent Enhancer	NHDF-Ad	bronchial
27	chr16:59427200-59431800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr16:59429200-59429600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr16:59429400-59429800	Enhancers	H1 Cell Line	embryonic stem cell
30	chr16:59429400-59430000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr16:59429400-59430200	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr16:59431800-59433200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr16:59432400-59433200	Enhancers	HUVEC	blood vessel
34	chr16:59433200-59434200	Weak transcription	HUVEC	blood vessel
35	chr16:59434200-59435400	Enhancers	HUVEC	blood vessel
36	chr16:59434600-59435600	Enhancers	A549	lung
37	chr16:59435600-59436800	Weak transcription	A549	lung
38	chr16:59436800-59437000	Enhancers	A549	lung
39	chr16:59445800-59446800	Enhancers	A549	lung
40	chr16:59446200-59446600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr16:59446400-59446800	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr16:59446800-59452000	Weak transcription	A549	lung
43	chr16:59454200-59454600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr16:59454200-59454600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr16:59465800-59467400	Enhancers	Fetal Brain Male	brain
46	chr16:59466800-59467200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr16:59467200-59467600	Enhancers	Brain Germinal Matrix	brain
48	chr16:59481000-59481400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr16:59493800-59494200	Enhancers	HUVEC	blood vessel
50	chr16:59494200-59497000	Weak transcription	HUVEC	blood vessel

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