Variant report

Variant	nsv817744
Chromosome Location	chr16:80989859-81027685
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:565)
CpG islands
(count:61)
Chromatin interactive
region (count:49)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:565 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:81008535-81008884	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:80992390-80992446	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:81024660-81024859	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:81024192-81024348	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:81002441-81002634	HepG2	liver:	n/a	n/a
6	ARID3A	chr16:81026852-81027349	K562	blood:	n/a	n/a
7	ARID3A	chr16:81026947-81027271	HepG2	liver:	n/a	n/a
8	ARID3A	chr16:81008565-81008842	K562	blood:	n/a	n/a
9	ARID3A	chr16:81025280-81026076	HepG2	liver:	n/a	n/a
10	ATF1	chr16:81026925-81027244	K562	blood:	n/a	n/a
11	BACH1	chr16:81021115-81021422	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr16:81021158-81021393	H1-hESC	embryonic stem cell:	n/a	n/a
13	BHLHE40	chr16:81026922-81027302	K562	blood:	n/a	n/a
14	BHLHE40	chr16:81008523-81008637	K562	blood:	n/a	n/a
15	BRCA1	chr16:81026384-81027436	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr16:81026802-81027336	K562	blood:	n/a	n/a
17	CCNT2	chr16:81026925-81027163	K562	blood:	n/a	n/a
18	CEBPB	chr16:81026953-81027268	HepG2	liver:	n/a	n/a
19	CEBPB	chr16:81018292-81018412	HepG2	liver:	n/a	chr16:81018321-81018332
20	CEBPB	chr16:81026971-81027174	K562	blood:	n/a	n/a
21	CEBPB	chr16:81026960-81027302	HepG2	liver:	n/a	n/a
22	CEBPB	chr16:81010913-81011187	IMR90	lung:	n/a	n/a
23	CEBPB	chr16:81012924-81012987	K562	blood:	n/a	n/a
24	CEBPB	chr16:81025451-81025664	HepG2	liver:	n/a	n/a
25	CEBPB	chr16:81001594-81001885	HepG2	liver:	n/a	n/a
26	CEBPB	chr16:81012894-81013182	IMR90	lung:	n/a	n/a
27	CEBPB	chr16:81026569-81027334	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr16:81026896-81027372	K562	blood:	n/a	n/a
29	CEBPB	chr16:81026870-81027364	A549	lung:	n/a	n/a
30	CEBPB	chr16:81018199-81018439	A549	lung:	n/a	chr16:81018321-81018332
31	CEBPB	chr16:81026931-81027328	IMR90	lung:	n/a	n/a
32	CEBPB	chr16:81026948-81027310	A549	lung:	n/a	n/a
33	CEBPB	chr16:81025422-81025793	HepG2	liver:	n/a	n/a
34	CEBPB	chr16:81026949-81027309	K562	blood:	n/a	n/a
35	CEBPD	chr16:81026792-81027282	K562	blood:	n/a	n/a
36	CHD2	chr16:81027177-81027219	K562	blood:	n/a	n/a
37	CHD2	chr16:81026867-81027241	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr16:81008940-81009090	HCFaa	heart:	n/a	n/a
39	CTCF	chr16:81008880-81008996	GM19240	blood:	n/a	chr16:81008888-81008904 chr16:81008889-81008910 chr16:81008890-81008903
40	CTCF	chr16:81008584-81008759	GM10248	blood:	n/a	n/a
41	CTCF	chr16:81008580-81008730	GM12868	blood:	n/a	n/a
42	CTCF	chr16:81002359-81002600	K562	blood:	n/a	n/a
43	CTCF	chr16:81009040-81009190	WI-38	lung:	n/a	n/a
44	CTCF	chr16:81008629-81008735	Lung_OC	lung:	n/a	n/a
45	CTCF	chr16:81008560-81008710	GM12872	blood:	n/a	n/a
46	CTCF	chr16:81008600-81008750	BE2_C	brain:	n/a	n/a
47	CTCF	chr16:81008576-81009042	MCF-7	breast:	n/a	chr16:81008888-81008904 chr16:81008889-81008910 chr16:81008890-81008903
48	CTCF	chr16:81008580-81008730	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr16:81022500-81022650	RPTEC	kidney:	n/a	n/a
50	CTCF	chr16:81008620-81008770	HCM	heart:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:81020862-81020912	IMR90	lung:	fetal
2	chr16:81020862-81020912	NB4	blood:	n/a
3	chr16:81020862-81020912	BE2_C	brain:	n/a
4	chr16:81020862-81020912	K562	blood:	n/a
5	chr16:81020862-81020912	HRPEpiC	eye:	n/a
6	chr16:81020862-81020912	HEEpiC	esophagus:	n/a
7	chr16:81020862-81020912	ovcar-3	ovarian:	n/a
8	chr16:81020862-81020912	HMEC	breast:	n/a
9	chr16:81020862-81020912	HEK293	kidney:	embryo
10	chr16:81020862-81020912	T-47D	breast:	n/a
11	chr16:81020862-81020912	HUVEC	blood vessel:	n/a
12	chr16:81020862-81020912	Caco-2	colon:	n/a
13	chr16:81020862-81020912	GM12892	blood:	n/a
14	chr16:81020862-81020912	Hepatocyte	liver:	n/a
15	chr16:81020862-81020912	GM12891	blood:	n/a
16	chr16:81020862-81020912	SKMC	muscle:	n/a
17	chr16:81020862-81020912	HepG2	liver:	n/a
18	chr16:81020862-81020912	HL-60	blood:	n/a
19	chr16:81020862-81020912	AoSMC	blood vessel:	n/a
20	chr16:81020862-81020912	Hela-S3	cervix:	n/a
21	chr16:81020862-81020912	AG04450	lung:	fetal
22	chr16:81020862-81020912	H1-hESC	embryonic stem cell:	embryo
23	chr16:81020862-81020912	Jurkat	blood:	n/a
24	chr16:81020862-81020912	ProgFib	skin:	n/a
25	chr16:81020862-81020912	MCF-7	breast:	n/a
26	chr16:81020862-81020912	GM12878	blood:	n/a
27	chr16:81020862-81020912	NT2-D1	testis:	n/a
28	chr16:81020862-81020912	HAEpiC	amniotic membrane:	n/a
29	chr16:81020862-81020912	A549	lung:	n/a
30	chr16:81020862-81020912	NHDF-neo	bronchial:	n/a
31	chr16:81020862-81020912	SAEC	small airway:	n/a
32	chr16:81020862-81020912	AG04449	skin:	fetal
33	chr16:81020862-81020912	AG09309	skin:	n/a
34	chr16:81020862-81020912	LNCaP	prostate:	n/a
35	chr16:81020862-81020912	MCF10A-Er-Src	breast:	n/a
36	chr16:81020862-81020912	HNPCEpiC	eye:	n/a
37	chr16:81020862-81020912	BJ	skin:	n/a
38	chr16:81020862-81020912	RPTEC	kidney:	n/a
39	chr16:81020862-81020912	GM06990	blood:	n/a
40	chr16:81020862-81020912	PrEC	prostate:	n/a
41	chr16:81020862-81020912	SK-N-SH	brain:	n/a
42	chr16:81020862-81020912	ECC-1	luminal epithelium:	n/a
43	chr16:81020862-81020912	GM19239	blood:	n/a
44	chr16:81020862-81020912	HCT-116	colon:	n/a
45	chr16:81020862-81020912	HCPEpiC	choroid plexus:	n/a
46	chr16:81020862-81020912	CMK	blood:	n/a
47	chr16:81020862-81020912	HCM	heart:	n/a
48	chr16:81020862-81020912	HPAEpiC	pulmonary alveolar:	n/a
49	chr16:81020862-81020912	HCF	heart:	n/a
50	chr16:81020862-81020912	NH-A	brain:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:81025833..81027865-chr16:81069028..81070871,2	K562	blood:
2	chr16:81008293..81009087-chr16:81022137..81022800,2	MCF-7	breast:
3	chr16:81009604..81011384-chr16:81022091..81025073,2	K562	blood:
4	chr16:81005392..81007770-chr16:81008815..81010427,2	K562	blood:
5	chr16:81001788..81003366-chr16:81003777..81008120,3	K562	blood:
6	chr16:81022564..81024564-chr16:81037053..81038818,2	K562	blood:
7	chr16:81009385..81010081-chr16:81069117..81069862,2	MCF-7	breast:
8	chr16:81010646..81012687-chr16:81017648..81020367,3	K562	blood:
9	chr16:80992891..80995365-chr16:80995391..80997695,2	MCF-7	breast:
10	chr16:81015364..81016919-chr16:81018878..81020602,2	K562	blood:
11	chr16:81008331..81009125-chr16:81068545..81069747,6	MCF-7	breast:
12	chr16:81011048..81013773-chr16:81013873..81016245,3	MCF-7	breast:
13	chr16:81026654..81030284-chr16:81073967..81077178,3	K562	blood:
14	chr16:81011971..81013927-chr16:81017238..81018745,2	MCF-7	breast:
15	chr16:81001788..81003366-chr16:81003777..81008120,3	K562	blood:
16	chr16:81008293..81009087-chr16:81022137..81022800,2	MCF-7	breast:
17	chr16:81017079..81020822-chr16:81021056..81026282,6	K562	blood:
18	chr16:81009884..81011946-chr16:81022091..81024291,2	K562	blood:
19	chr16:81019105..81021887-chr16:81039011..81042107,3	MCF-7	breast:
20	chr16:81005392..81007770-chr16:81008815..81010427,2	K562	blood:
21	chr16:81006336..81010251-chr16:81016347..81019319,3	K562	blood:
22	chr16:81009884..81011946-chr16:81022091..81024291,2	K562	blood:
23	chr16:81006720..81008991-chr16:81041065..81043268,2	MCF-7	breast:
24	chr16:81023827..81025532-chr16:81042311..81045114,2	K562	blood:
25	chr16:81022346..81024117-chr16:81029726..81031989,2	K562	blood:
26	chr16:81007590..81009506-chr16:81039765..81041887,2	MCF-7	breast:
27	chr16:81010646..81012687-chr16:81017648..81020367,3	K562	blood:
28	chr16:81000562..81002901-chr16:81037638..81039411,2	K562	blood:
29	chr16:81002503..81003109-chr16:81069304..81069808,2	K562	blood:
30	chr16:81005749..81007620-chr16:81026993..81029850,2	K562	blood:
31	chr16:81025473..81027772-chr16:81037035..81041311,4	K562	blood:
32	chr16:81025909..81029223-chr16:81033494..81036388,3	K562	blood:
33	chr16:81006406..81009066-chr16:81012697..81014236,2	K562	blood:
34	chr16:81007739..81010251-chr16:81016347..81018529,2	K562	blood:
35	chr16:81015364..81016919-chr16:81018878..81020602,2	K562	blood:
36	chr16:81011048..81013773-chr16:81013873..81016245,3	MCF-7	breast:
37	chr16:81023188..81026086-chr16:81027867..81032620,4	MCF-7	breast:
38	chr16:81011817..81018316-chr16:81020382..81024504,8	MCF-7	breast:
39	chr16:81021689..81024078-chr16:81024702..81027274,2	MCF-7	breast:
40	chr16:80992093..80994381-chr16:81038938..81040889,2	MCF-7	breast:
41	chr16:80992891..80995365-chr16:80995391..80997695,2	MCF-7	breast:
42	chr16:81011971..81013927-chr16:81017238..81018745,2	MCF-7	breast:
43	chr16:81016839..81018577-chr16:81026525..81028727,2	MCF-7	breast:
44	chr16:81005749..81007620-chr16:81026993..81029850,2	K562	blood:
45	chr16:81004010..81005994-chr16:81040056..81041690,2	K562	blood:
46	chr16:81009604..81011384-chr16:81022091..81025073,2	K562	blood:
47	chr16:81006406..81009066-chr16:81012697..81014236,2	K562	blood:
48	chr16:81007937..81010698-chr16:81068486..81070530,2	MCF-7	breast:
49	chr16:81008172..81008838-chr16:89926929..89927458,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C16orf61-3	chr16:81009701-81010076	NONHSAT143921
2	lnc-C16orf61-3	chr16:81009701-81010076	NONHSAT143920
3	lnc-C16orf61-3	chr16:81014375-81014484	NONHSAT143920
4	lnc-C16orf61-3	chr16:81009699-81010076	NONHSAT143918
5	lnc-C16orf61-3	chr16:81014435-81014484	NONHSAT143925
6	lnc-C16orf61-3	chr16:81015411-81015482	NONHSAT143921
7	lnc-C16orf61-3	chr16:81015411-81015482	NONHSAT143918
8	lnc-C16orf61-3	chr16:81025359-81025560	NONHSAT143918
9	lnc-C16orf61-3	chr16:81009701-81010076	NONHSAT143922
10	lnc-CENPN-1	chr16:81003707-81005460	NONHSAT143915
11	lnc-C16orf61-3	chr16:81015411-81015482	NONHSAT143925

No data

Variant related genes	Relation type
CMC2	TF binding region
CMC2	CpG island
ENSG00000166451	chromatin interactions
ENSG00000103121	chromatin interactions
ENSG00000166454	chromatin interactions
ENSG00000260213	chromatin interactions

Extended variants
information (count: 2104 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:2104 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9924198	chr16:80989859-80989860	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs75494692	chr16:80989885-80989886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566029106	chr16:80989892-80989893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535884960	chr16:80989898-80989899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs9924824	chr16:80989900-80989901	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs192564818	chr16:80989909-80989910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537115323	chr16:80989910-80989911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184492575	chr16:80989912-80989913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547844478	chr16:80989939-80989940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577065308	chr16:80989941-80989942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369241228	chr16:80989967-80989968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35814745	chr16:80990000-80990001	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs572194553	chr16:80990014-80990015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs189169106	chr16:80990020-80990021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530547451	chr16:80990025-80990026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs35134411	chr16:80990052-80990053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs144591911	chr16:80990056-80990057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs35237667	chr16:80990089-80990090	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs561310228	chr16:80990106-80990107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531725984	chr16:80990108-80990109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192670619	chr16:80990111-80990112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs34403022	chr16:80990121-80990122	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs539279769	chr16:80990146-80990147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs199618986	chr16:80990149-80990150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112515119	chr16:80990157-80990158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113979880	chr16:80990160-80990161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs34947891	chr16:80990193-80990194	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs566065917	chr16:80990199-80990200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112512737	chr16:80990204-80990205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547898218	chr16:80990211-80990212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs35848471	chr16:80990218-80990219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148488474	chr16:80990220-80990221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs386792823	chr16:80990266-80990267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs114638119	chr16:80990267-80990268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570553118	chr16:80990288-80990289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs144080897	chr16:80990329-80990330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374234319	chr16:80990383-80990384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537197110	chr16:80990416-80990417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553185537	chr16:80990449-80990450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574809917	chr16:80990461-80990462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs111343506	chr16:80990463-80990464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554673621	chr16:80990469-80990470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577170395	chr16:80990538-80990539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371014588	chr16:80990552-80990553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs576336694	chr16:80990595-80990596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543447692	chr16:80990596-80990597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184657757	chr16:80990642-80990643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs13339107	chr16:80990644-80990645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs146489545	chr16:80990730-80990731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577615014	chr16:80990750-80990751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
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
Autism	22495311	CNVD
Wilms tumour	21544195	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
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	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
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	21865298	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Neuroblastoma	18923524	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Obesity	20622171	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:943 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:80989400-81008800	Weak transcription	Gastric	stomach
2	chr16:80989800-80991400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr16:80994200-80994800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr16:80994600-81007800	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr16:80994600-81026400	Weak transcription	HSMMtube	muscle
6	chr16:80994800-81023400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr16:80995400-81003200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr16:80996000-80996200	ZNF genes & repeats	Aorta	Aorta
9	chr16:80996000-81007400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr16:80996200-81008600	Weak transcription	Aorta	Aorta
11	chr16:80996600-81018600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr16:80997800-81008800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr16:80998000-80998200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr16:80998000-80998400	Active TSS	NHDF-Ad	bronchial
15	chr16:80998000-80998400	Active TSS	Osteobl	bone
16	chr16:80998000-81003200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr16:80998000-81004000	Weak transcription	HSMM	muscle
18	chr16:80998000-81009600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr16:80998200-80999000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr16:80998200-81009400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr16:80998200-81013800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr16:80998400-80998600	Enhancers	GM12878-XiMat	blood
23	chr16:80998400-80998600	Enhancers	NHDF-Ad	bronchial
24	chr16:80998400-80998800	Enhancers	Osteobl	bone
25	chr16:80998400-81030800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr16:80998600-81005800	Weak transcription	GM12878-XiMat	blood
27	chr16:80998600-81008000	Weak transcription	NHDF-Ad	bronchial
28	chr16:80998600-81014800	Weak transcription	Brain Angular Gyrus	brain
29	chr16:80998800-81002200	Weak transcription	Osteobl	bone
30	chr16:80999000-81002400	Weak transcription	A549	lung
31	chr16:80999000-81003200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr16:80999400-81003000	Weak transcription	Hela-S3	cervix
33	chr16:81000000-81000200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr16:81000000-81000200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr16:81000000-81000200	Enhancers	NHEK	skin
36	chr16:81000000-81001200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr16:81000200-81001000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr16:81000200-81006600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr16:81000200-81007800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr16:81000200-81008000	Weak transcription	NHEK	skin
41	chr16:81000400-81002600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr16:81000600-81003000	Weak transcription	Fetal Stomach	stomach
43	chr16:81000800-81002600	Weak transcription	Primary T cells from cord blood	blood
44	chr16:81000800-81002600	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr16:81001000-81002800	Weak transcription	Brain Substantia Nigra	brain
46	chr16:81001000-81004000	Weak transcription	Primary T helper cells PMA-I stimulated	--
47	chr16:81001000-81005800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr16:81001000-81020400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr16:81001200-81003000	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chr16:81001200-81004000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links