Variant report

Variant	nsv524636
Chromosome Location	chr16:77258592-77297193
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:525)
CpG islands
(count:244)
Chromatin interactive
region (count:34)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:525 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:77269941-77270279	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:77265478-77265545	K562	blood:	n/a	n/a
3	ARID3A	chr16:77265076-77265272	K562	blood:	n/a	n/a
4	ATF1	chr16:77264998-77265300	K562	blood:	n/a	n/a
5	ATF1	chr16:77269929-77270421	K562	blood:	n/a	n/a
6	ATF2	chr16:77269965-77270273	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr16:77269872-77270385	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr16:77261647-77261980	GM12878	blood:	n/a	n/a
9	ATF3	chr16:77264959-77265251	K562	blood:	n/a	n/a
10	ATF3	chr16:77269841-77270350	A549	lung:	n/a	n/a
11	ATF3	chr16:77269974-77270281	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr16:77269998-77270283	HepG2	liver:	n/a	n/a
13	ATF3	chr16:77269869-77270401	A549	lung:	n/a	n/a
14	BACH1	chr16:77296164-77296240	K562	blood:	n/a	n/a
15	BATF	chr16:77261626-77262016	GM12878	blood:	n/a	chr16:77261853-77261864
16	BATF	chr16:77261616-77262039	GM12878	blood:	n/a	chr16:77261853-77261864
17	BCLAF1	chr16:77269900-77270330	GM12878	blood:	n/a	n/a
18	BHLHE40	chr16:77269862-77270298	K562	blood:	n/a	n/a
19	BHLHE40	chr16:77269914-77270288	HepG2	liver:	n/a	n/a
20	BHLHE40	chr16:77269962-77270356	GM12878	blood:	n/a	n/a
21	BHLHE40	chr16:77265078-77265672	K562	blood:	n/a	n/a
22	BRCA1	chr16:77269949-77270334	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr16:77268531-77268857	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr16:77269938-77270250	HepG2	liver:	n/a	n/a
25	CBX3	chr16:77269940-77270289	K562	blood:	n/a	n/a
26	CCNT2	chr16:77264930-77265244	K562	blood:	n/a	chr16:77265082-77265102
27	CEBPB	chr16:77265018-77265213	K562	blood:	n/a	n/a
28	CEBPB	chr16:77265413-77265651	HepG2	liver:	n/a	chr16:77265561-77265572 chr16:77265561-77265574 chr16:77265465-77265478 chr16:77265495-77265508
29	CEBPB	chr16:77269966-77270290	K562	blood:	n/a	n/a
30	CEBPB	chr16:77269865-77270370	MCF-7	breast:	n/a	n/a
31	CEBPB	chr16:77264916-77265353	K562	blood:	n/a	n/a
32	CEBPB	chr16:77261112-77261359	HepG2	liver:	n/a	chr16:77261253-77261264
33	CEBPB	chr16:77265032-77265604	K562	blood:	n/a	chr16:77265561-77265572 chr16:77265561-77265574 chr16:77265465-77265478 chr16:77265495-77265508
34	CEBPB	chr16:77269948-77270349	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr16:77261111-77261348	A549	lung:	n/a	chr16:77261253-77261264
36	CEBPB	chr16:77269929-77270333	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr16:77269956-77270305	HepG2	liver:	n/a	n/a
38	CEBPB	chr16:77297176-77297177	HepG2	liver:	n/a	n/a
39	CEBPB	chr16:77269967-77270315	A549	lung:	n/a	n/a
40	CEBPB	chr16:77269971-77270283	IMR90	lung:	n/a	n/a
41	CEBPD	chr16:77264886-77265279	K562	blood:	n/a	n/a
42	CHD1	chr16:77269940-77270436	IMR90	lung:	n/a	n/a
43	CHD2	chr16:77268568-77268688	K562	blood:	n/a	n/a
44	CHD2	chr16:77269907-77270311	HepG2	liver:	n/a	n/a
45	CHD2	chr16:77269917-77270299	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr16:77268484-77268839	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr16:77270020-77270331	K562	blood:	n/a	n/a
48	CHD2	chr16:77269941-77270369	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr16:77269909-77270437	HepG2	liver:	n/a	n/a
50	CREB1	chr16:77269884-77270483	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:77270312-77270362	HRCEpiC	kidney:	n/a
2	chr16:77270156-77270206	HRPEpiC	eye:	n/a
3	chr16:77270156-77270206	ECC-1	luminal epithelium:	n/a
4	chr16:77270312-77270362	BE2_C	brain:	n/a
5	chr16:77272123-77272173	SK-N-MC	brain:	n/a
6	chr16:77272123-77272173	T-47D	breast:	n/a
7	chr16:77272123-77272173	NHBE	bronchial:	n/a
8	chr16:77272123-77272173	Hepatocyte	liver:	n/a
9	chr16:77270312-77270362	HEK293	kidney:	embryo
10	chr16:77270312-77270362	ovcar-3	ovarian:	n/a
11	chr16:77270057-77270107	HRE	kidney:	n/a
12	chr16:77270312-77270362	SKMC	muscle:	n/a
13	chr16:77270057-77270107	HAEpiC	amniotic membrane:	n/a
14	chr16:77270156-77270206	HCT-116	colon:	n/a
15	chr16:77270057-77270107	GM12892	blood:	n/a
16	chr16:77270312-77270362	H1-hESC	embryonic stem cell:	embryo
17	chr16:77272123-77272173	ProgFib	skin:	n/a
18	chr16:77270057-77270107	NHBE	bronchial:	n/a
19	chr16:77272123-77272173	GM19239	blood:	n/a
20	chr16:77270312-77270362	GM12892	blood:	n/a
21	chr16:77270057-77270107	GM06990	blood:	n/a
22	chr16:77270312-77270362	HEEpiC	esophagus:	n/a
23	chr16:77272123-77272173	GM12891	blood:	n/a
24	chr16:77272123-77272173	SAEC	small airway:	n/a
25	chr16:77272123-77272173	HRPEpiC	eye:	n/a
26	chr16:77270057-77270107	Hela-S3	cervix:	n/a
27	chr16:77270057-77270107	CMK	blood:	n/a
28	chr16:77270312-77270362	T-47D	breast:	n/a
29	chr16:77270312-77270362	GM19239	blood:	n/a
30	chr16:77270312-77270362	SK-N-MC	brain:	n/a
31	chr16:77270156-77270206	Caco-2	colon:	n/a
32	chr16:77270057-77270107	PFSK-1	brain:	n/a
33	chr16:77270156-77270206	IMR90	lung:	fetal
34	chr16:77270156-77270206	AG04449	skin:	fetal
35	chr16:77270057-77270107	HepG2	liver:	n/a
36	chr16:77270156-77270206	HPAEpiC	pulmonary alveolar:	n/a
37	chr16:77270057-77270107	HPAEpiC	pulmonary alveolar:	n/a
38	chr16:77270057-77270107	NH-A	brain:	n/a
39	chr16:77270156-77270206	HCPEpiC	choroid plexus:	n/a
40	chr16:77270156-77270206	CMK	blood:	n/a
41	chr16:77270156-77270206	Hela-S3	cervix:	n/a
42	chr16:77272123-77272173	HL-60	blood:	n/a
43	chr16:77270156-77270206	HCF	heart:	n/a
44	chr16:77270312-77270362	CMK	blood:	n/a
45	chr16:77272123-77272173	HUVEC	blood vessel:	n/a
46	chr16:77272123-77272173	SK-N-SH	brain:	n/a
47	chr16:77272123-77272173	RPTEC	kidney:	n/a
48	chr16:77270156-77270206	HEK293	kidney:	embryo
49	chr16:77270312-77270362	SAEC	small airway:	n/a
50	chr16:77270312-77270362	AG09319	gingival:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:77269653..77270243-chr16:77410066..77410842,2	MCF-7	breast:
2	chr16:77278039..77279706-chr16:77282947..77285823,2	K562	blood:
3	chr16:77269714..77270636-chr16:78005192..78006113,3	MCF-7	breast:
4	chr16:77269442..77270538-chr16:77616365..77617604,8	MCF-7	breast:
5	chr16:77273435..77275318-chr16:77277806..77279543,2	K562	blood:
6	chr16:77059610..77062396-chr16:77260233..77262257,2	K562	blood:
7	chr16:77269601..77270543-chr16:78127747..78128804,5	MCF-7	breast:
8	chr16:77253600..77256492-chr16:77257783..77260581,2	MCF-7	breast:
9	chr16:77284002..77285688-chr16:77295972..77298884,2	K562	blood:
10	chr16:77272210..77274074-chr16:77274848..77276785,2	K562	blood:
11	chr16:77269587..77270650-chr16:77693914..77694941,6	MCF-7	breast:
12	chr16:77269742..77270569-chr16:77620970..77621576,2	K562	blood:
13	chr16:77269244..77270388-chr16:78133563..78134543,4	MCF-7	breast:
14	chr16:77269829..77270541-chr16:78156421..78156984,2	MCF-7	breast:
15	chr16:77269656..77270610-chr16:77471829..77472511,2	MCF-7	breast:
16	chr16:77269705..77270364-chr16:77617639..77618395,2	MCF-7	breast:
17	chr16:77269710..77270493-chr16:77407930..77408448,2	MCF-7	breast:
18	chr16:77269912..77270651-chr16:77440233..77440965,2	MCF-7	breast:
19	chr16:77269609..77270743-chr16:77617331..77618809,19	MCF-7	breast:
20	chr16:77284002..77285688-chr16:77295972..77298884,2	K562	blood:
21	chr16:77269674..77270537-chr16:77630372..77631796,5	MCF-7	breast:
22	chr16:77269648..77270617-chr16:77633407..77634157,3	MCF-7	breast:
23	chr16:77269122..77270769-chr16:77617508..77619193,29	K562	blood:
24	chr16:77269847..77270615-chr16:78036552..78037506,3	MCF-7	breast:
25	chr16:77272210..77274074-chr16:77274848..77276785,2	K562	blood:
26	chr16:77270827..77273533-chr16:77609771..77611540,2	K562	blood:
27	chr16:77273139..77275298-chr16:77332609..77335095,2	MCF-7	breast:
28	chr16:77269595..77270510-chr16:78004909..78005878,4	K562	blood:
29	chr16:77270739..77273458-chr16:77636094..77637749,2	MCF-7	breast:
30	chr16:77273435..77275318-chr16:77277806..77279543,2	K562	blood:
31	chr16:77269962..77270537-chr16:77619167..77620058,2	MCF-7	breast:
32	chr16:77269675..77270630-chr16:77694031..77695259,6	MCF-7	breast:
33	chr16:77269940..77270623-chr16:77616328..77616995,3	K562	blood:
34	chr16:77269758..77270518-chr16:77334286..77335046,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAMTS18-1	chr16:77283791-77283854	ENSG00000261063.1

No data

Variant related genes	Relation type
ENSG00000260922	TF binding region
ENSG00000261063	TF binding region
ENSG00000260922	CpG island
ENSG00000261063	CpG island
ENSG00000186153	chromatin interactions
ENSG00000226348	chromatin interactions
ENSG00000261063	chromatin interactions

Extended variants
information (count: 1983 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1983 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9922281	chr16:77258592-77258593	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530723024	chr16:77258619-77258620	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs145567142	chr16:77258623-77258624	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs6564413	chr16:77258687-77258688	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs140320969	chr16:77258755-77258756	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs549533469	chr16:77258767-77258768	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs199707516	chr16:77258777-77258778	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs9922441	chr16:77258780-77258781	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs535093345	chr16:77258785-77258786	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs558073415	chr16:77258789-77258790	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs9932327	chr16:77258834-77258835	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs183002876	chr16:77258853-77258854	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs78933654	chr16:77258865-77258866	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
14	rs573333721	chr16:77258866-77258867	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs144314659	chr16:77258867-77258868	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs74485818	chr16:77258889-77258890	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs572605580	chr16:77258899-77258900	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs554906269	chr16:77258907-77258908	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs564948083	chr16:77258929-77258930	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs368052395	chr16:77258930-77258931	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs372502467	chr16:77258948-77258949	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs7184316	chr16:77258967-77258968	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs530729646	chr16:77258972-77258973	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs141288016	chr16:77258986-77258987	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs561152407	chr16:77258987-77258988	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs369761717	chr16:77259012-77259013	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs529982202	chr16:77259018-77259019	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs537498706	chr16:77259046-77259047	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs549422420	chr16:77259060-77259061	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs559738628	chr16:77259080-77259081	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs528608835	chr16:77259104-77259105	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs374327508	chr16:77259113-77259114	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs551845985	chr16:77259127-77259128	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs553382155	chr16:77259188-77259189	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs7184720	chr16:77259211-77259212	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs550858830	chr16:77259238-77259239	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs567639654	chr16:77259240-77259241	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs536498532	chr16:77259249-77259250	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs67076559	chr16:77259250-77259251	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs572494670	chr16:77259281-77259282	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs143254737	chr16:77259288-77259289	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs148296152	chr16:77259296-77259297	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs76016205	chr16:77259307-77259308	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs544411639	chr16:77259320-77259321	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs561037542	chr16:77259365-77259366	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs140647371	chr16:77259370-77259371	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs150469714	chr16:77259383-77259384	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs7195139	chr16:77259396-77259397	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs528486718	chr16:77259451-77259452	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs78691637	chr16:77259535-77259536	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Lung cancer	24585490	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20581869	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
early-passage human iPS cells	21368824	CNVD
Melanoma	17363583	CNVD
Ovarian cancer	21720365	CNVD
Bipolar disorder	19114987	CNVD
Barrett''s syndrome	19417022	CNVD
Colorectal cancer	22860045	CNVD
Gastric cancer	22315472	CNVD

Chromatin state (count:217 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:77247800-77261600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr16:77248800-77262000	Weak transcription	Fetal Muscle Trunk	muscle
3	chr16:77254800-77260000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr16:77255600-77261000	Weak transcription	A549	lung
5	chr16:77257200-77259200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr16:77257600-77268000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr16:77258200-77258600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr16:77258200-77258600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr16:77258200-77258600	Bivalent Enhancer	Osteobl	bone
10	chr16:77258200-77258800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr16:77258400-77258600	Enhancers	Brain Angular Gyrus	brain
12	chr16:77258400-77258800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr16:77259200-77269800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr16:77260000-77260200	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr16:77261000-77261400	Enhancers	A549	lung
16	chr16:77261400-77270200	Weak transcription	A549	lung
17	chr16:77261600-77261800	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr16:77261600-77262200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr16:77261600-77262400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr16:77261600-77262600	Enhancers	GM12878-XiMat	blood
21	chr16:77261800-77262200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr16:77262000-77262200	Enhancers	Fetal Lung	lung
23	chr16:77262200-77262400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr16:77262200-77262800	Enhancers	Fetal Stomach	stomach
25	chr16:77262400-77263000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr16:77262400-77271200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr16:77268000-77268200	Enhancers	H1 Cell Line	embryonic stem cell
28	chr16:77268000-77269200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr16:77268200-77268600	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr16:77268200-77269200	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr16:77268200-77269800	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr16:77268200-77270200	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr16:77268400-77268800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr16:77268400-77269200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr16:77268400-77269200	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr16:77268600-77268800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr16:77268600-77268800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr16:77268600-77268800	Enhancers	HUVEC	blood vessel
39	chr16:77268600-77269000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
40	chr16:77268800-77269000	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
41	chr16:77268800-77269000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr16:77268800-77269000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr16:77268800-77269800	Weak transcription	HUVEC	blood vessel
44	chr16:77268800-77270000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr16:77269000-77269200	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr16:77269200-77269600	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr16:77269200-77269600	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr16:77269200-77269600	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr16:77269200-77270200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr16:77269600-77270200	Enhancers	HUES48 Cell Line	embryonic stem cell

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