Variant report

Variant	nsv878535
Chromosome Location	chr4:7093834-7135912
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:932)
CpG islands
(count:1165)
Chromatin interactive
region (count:40)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:932 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr4:7122098-7122348	K562	blood:	n/a	n/a
2	BACH1	chr4:7105314-7105465	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr4:7133556-7133887	GM12878	blood:	n/a	n/a
4	BCL3	chr4:7135011-7135294	GM12878	blood:	n/a	n/a
5	BCL3	chr4:7133549-7133962	GM12878	blood:	n/a	n/a
6	BHLHE40	chr4:7103743-7104167	K562	blood:	n/a	n/a
7	BHLHE40	chr4:7126714-7127101	K562	blood:	n/a	n/a
8	BHLHE40	chr4:7103753-7104166	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:7107217-7107412	K562	blood:	n/a	n/a
10	BHLHE40	chr4:7105183-7105776	HepG2	liver:	n/a	n/a
11	BHLHE40	chr4:7104815-7104956	K562	blood:	n/a	n/a
12	BHLHE40	chr4:7129826-7130186	K562	blood:	n/a	chr4:7130017-7130026
13	BHLHE40	chr4:7129458-7129606	K562	blood:	n/a	n/a
14	BHLHE40	chr4:7105336-7105646	K562	blood:	n/a	n/a
15	BRCA1	chr4:7105407-7105588	HepG2	liver:	n/a	n/a
16	BRCA1	chr4:7105871-7105910	HepG2	liver:	n/a	n/a
17	CBX3	chr4:7134741-7135064	K562	blood:	n/a	n/a
18	CBX3	chr4:7134685-7135077	K562	blood:	n/a	n/a
19	CCNT2	chr4:7104691-7105294	K562	blood:	n/a	n/a
20	CEBPB	chr4:7126761-7127241	IMR90	lung:	n/a	chr4:7127078-7127089
21	CEBPB	chr4:7126425-7126668	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr4:7108245-7108467	IMR90	lung:	n/a	chr4:7108367-7108378
23	CEBPB	chr4:7108265-7108459	K562	blood:	n/a	chr4:7108367-7108378
24	CEBPB	chr4:7096011-7096198	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:7127867-7128099	HepG2	liver:	n/a	chr4:7127957-7127968
26	CEBPB	chr4:7124201-7124223	K562	blood:	n/a	chr4:7124210-7124223
27	CEBPB	chr4:7127760-7128075	K562	blood:	n/a	chr4:7127957-7127968
28	CEBPB	chr4:7108227-7108494	HepG2	liver:	n/a	chr4:7108367-7108378
29	CEBPB	chr4:7127770-7128098	K562	blood:	n/a	chr4:7127957-7127968
30	CEBPB	chr4:7095986-7096192	IMR90	lung:	n/a	n/a
31	CEBPD	chr4:7103881-7104207	HepG2	liver:	n/a	n/a
32	CEBPD	chr4:7104915-7105175	HepG2	liver:	n/a	n/a
33	CHD2	chr4:7104789-7104974	K562	blood:	n/a	n/a
34	CHD2	chr4:7122096-7122393	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr4:7104986-7105031	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr4:7105020-7105542	HepG2	liver:	n/a	n/a
37	CHD2	chr4:7122140-7122405	K562	blood:	n/a	n/a
38	CHD2	chr4:7104819-7105480	Hela-S3	cervix:	n/a	n/a
39	CREB1	chr4:7104884-7105175	A549	lung:	n/a	n/a
40	CTCF	chr4:7103800-7103950	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr4:7126869-7127009	MCF-7	breast:	n/a	n/a
42	CTCF	chr4:7104740-7104890	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:7104815-7104914	K562	blood:	n/a	n/a
44	CTCF	chr4:7123140-7123290	HepG2	liver:	n/a	chr4:7123194-7123207 chr4:7123192-7123210
45	CTCF	chr4:7135540-7135690	NHEK	skin:	n/a	n/a
46	CTCF	chr4:7132377-7133247	GM19239	blood:	n/a	n/a
47	CTCF	chr4:7103860-7104010	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr4:7103786-7104011	GM10248	blood:	n/a	n/a
49	CTCF	chr4:7132411-7132533	GM12891	blood:	n/a	n/a
50	CTCF	chr4:7103880-7104030	HL-60	blood:	n/a	n/a

(count:1165 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7129517-7129567	HL-60	blood:	n/a
2	chr4:7131061-7131111	BJ	skin:	n/a
3	chr4:7114046-7114096	HRE	kidney:	n/a
4	chr4:7131136-7131186	NHBE	bronchial:	n/a
5	chr4:7114067-7114117	AG10803	skin:	n/a
6	chr4:7131403-7131453	HIPEpiC	eye:	n/a
7	chr4:7129517-7129567	HL-60	blood:	n/a
8	chr4:7131061-7131111	BJ	skin:	n/a
9	chr4:7114046-7114096	HRE	kidney:	n/a
10	chr4:7131136-7131186	NHBE	bronchial:	n/a
11	chr4:7114067-7114117	AG10803	skin:	n/a
12	chr4:7131403-7131453	HIPEpiC	eye:	n/a
13	chr4:7129517-7129567	GM12891	blood:	n/a
14	chr4:7131403-7131453	MCF-7	breast:	n/a
15	chr4:7105272-7105322	GM12891	blood:	n/a
16	chr4:7131247-7131297	BE2_C	brain:	n/a
17	chr4:7105262-7105312	SK-N-SH	brain:	n/a
18	chr4:7114012-7114062	Hela-S3	cervix:	n/a
19	chr4:7126882-7126932	Hela-S3	cervix:	n/a
20	chr4:7104897-7104947	AoSMC	blood vessel:	n/a
21	chr4:7114046-7114096	GM19239	blood:	n/a
22	chr4:7131403-7131453	HRCEpiC	kidney:	n/a
23	chr4:7105272-7105322	ECC-1	luminal epithelium:	n/a
24	chr4:7131403-7131453	GM12891	blood:	n/a
25	chr4:7105115-7105165	SK-N-MC	brain:	n/a
26	chr4:7114012-7114062	HL-60	blood:	n/a
27	chr4:7131478-7131528	ProgFib	skin:	n/a
28	chr4:7105573-7105623	ProgFib	skin:	n/a
29	chr4:7105262-7105312	HL-60	blood:	n/a
30	chr4:7131061-7131111	SKMC	muscle:	n/a
31	chr4:7105262-7105312	AG09309	skin:	n/a
32	chr4:7131478-7131528	AG04449	skin:	fetal
33	chr4:7106195-7106245	HCF	heart:	n/a
34	chr4:7131061-7131111	K562	blood:	n/a
35	chr4:7105573-7105623	HRCEpiC	kidney:	n/a
36	chr4:7114012-7114062	HCM	heart:	n/a
37	chr4:7104195-7104245	PANC-1	pancreas:	n/a
38	chr4:7114046-7114096	HCF	heart:	n/a
39	chr4:7131061-7131111	HRCEpiC	kidney:	n/a
40	chr4:7131061-7131111	HMEC	breast:	n/a
41	chr4:7131478-7131528	K562	blood:	n/a
42	chr4:7105272-7105322	ovcar-3	ovarian:	n/a
43	chr4:7106195-7106245	IMR90	lung:	fetal
44	chr4:7131478-7131528	PFSK-1	brain:	n/a
45	chr4:7131136-7131186	NHDF-neo	bronchial:	n/a
46	chr4:7131478-7131528	ECC-1	luminal epithelium:	n/a
47	chr4:7104897-7104947	HL-60	blood:	n/a
48	chr4:7114012-7114062	Caco-2	colon:	n/a
49	chr4:7114046-7114096	AG09309	skin:	n/a
50	chr4:7106023-7106073	ProgFib	skin:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:7105147..7106911-chr4:7141540..7143652,2	K562	blood:
2	chr4:7114517..7116267-chr4:7117721..7119678,2	K562	blood:
3	chr4:7043790..7046279-chr4:7102506..7105292,2	K562	blood:
4	chr4:7120740..7122988-chr4:7129086..7130661,2	MCF-7	breast:
5	chr4:7077408..7080531-chr4:7105216..7108085,3	K562	blood:
6	chr4:7115313..7118277-chr4:7121147..7123527,2	MCF-7	breast:
7	chr4:7105809..7107677-chr4:7109830..7111435,2	K562	blood:
8	chr4:7083980..7086191-chr4:7094533..7096477,2	K562	blood:
9	chr4:7105809..7107677-chr4:7109830..7111435,2	K562	blood:
10	chr4:7098558..7101540-chr4:7102623..7104219,2	MCF-7	breast:
11	chr4:7103913..7106622-chr4:7111535..7115141,3	K562	blood:
12	chr4:7103774..7104291-chr4:7158329..7158835,2	MCF-7	breast:
13	chr4:7097658..7100396-chr4:7102280..7105139,5	K562	blood:
14	chr4:7106689..7108245-chr4:7109405..7112071,2	MCF-7	breast:
15	chr4:7088413..7090570-chr4:7093679..7095355,2	K562	blood:
16	chr4:7127382..7129975-chr4:7130114..7132149,2	MCF-7	breast:
17	chr4:7121664..7124511-chr4:7134767..7137572,2	K562	blood:
18	chr4:7105423..7108283-chr4:7118442..7120103,2	MCF-7	breast:
19	chr4:7124347..7127288-chr4:7130183..7132382,4	K562	blood:
20	chr4:7098558..7101540-chr4:7102623..7104219,2	MCF-7	breast:
21	chr4:7120740..7122988-chr4:7129086..7130661,2	MCF-7	breast:
22	chr4:7103610..7105955-chr4:7121635..7124295,2	K562	blood:
23	chr4:7093602..7095834-chr4:7100410..7102327,2	MCF-7	breast:
24	chr4:7105423..7108283-chr4:7118442..7120103,2	MCF-7	breast:
25	chr4:7096598..7098168-chr4:7102324..7105190,2	MCF-7	breast:
26	chr4:7114517..7116267-chr4:7117721..7119678,2	K562	blood:
27	chr4:7121664..7124511-chr4:7134767..7137572,2	K562	blood:
28	chr4:7093602..7095834-chr4:7100410..7102327,2	MCF-7	breast:
29	chr4:7106689..7108245-chr4:7109405..7112071,2	MCF-7	breast:
30	chr4:7099425..7101930-chr4:7102267..7105259,4	MCF-7	breast:
31	chr4:7103913..7106622-chr4:7111535..7115141,3	K562	blood:
32	chr4:7127382..7129975-chr4:7130114..7132149,2	MCF-7	breast:
33	chr4:7067941..7072292-chr4:7099619..7103393,4	MCF-7	breast:
34	chr4:7103913..7105517-chr4:7112314..7115141,2	K562	blood:
35	chr4:7125529..7126029-chr6:30710536..30711392,2	Hela-S3	cervix:
36	chr4:6783899..6786313-chr4:7103315..7105730,2	K562	blood:
37	chr4:7096026..7100396-chr4:7102325..7105652,7	K562	blood:
38	chr4:7103913..7105517-chr4:7112314..7115141,2	K562	blood:
39	chr4:7124347..7127288-chr4:7130183..7132382,4	K562	blood:
40	chr4:7115313..7118277-chr4:7121147..7123527,2	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRPEL1-1	chr4:7099050-7099106	ENSG00000245562
2	lnc-GRPEL1-2	chr4:7132819-7133131	XLOC_003873
3	lnc-GRPEL1-2	chr4:7133632-7133655	NONHSAT095050
4	lnc-GRPEL1-1	chr4:7096298-7096470	ENSG00000245562
5	lnc-GRPEL1-1	chr4:7099050-7099106	NONHSAT095046
6	lnc-GRPEL1-1	chr4:7104995-7105139	NONHSAT095046
7	lnc-GRPEL1-1	chr4:7104995-7105186	XLOC_003872
8	lnc-GRPEL1-1	chr4:7102967-7105112	ENSG00000245468
9	lnc-GRPEL1-2	chr4:7132607-7132626	XLOC_003873
10	lnc-GRPEL1-1	chr4:7104995-7105107	ENSG00000245562
11	lnc-GRPEL1-1	chr4:7099080-7099106	XLOC_003872
12	lnc-GRPEL1-1	chr4:7099795-7101181	ENSG00000245562
13	lnc-GRPEL1-2	chr4:7132540-7133055	NONHSAT095050
14	lnc-GRPEL1-1	chr4:7104995-7105103	XLOC_003872
15	lnc-GRPEL1-1	chr4:7096326-7096470	NONHSAT095046
16	lnc-GRPEL1-1	chr4:7099151-7101181	XLOC_003872
17	lnc-GRPEL1-1	chr4:7104995-7105056	ENSG00000245562

No data

Variant related genes	Relation type
ENSG00000245468	TF binding region
RN7SKP36	TF binding region
ENSG00000245468	CpG island
RN7SKP36	CpG island
ENSG00000170871	chromatin interactions
ENSG00000272273	chromatin interactions
ENSG00000173013	chromatin interactions
ENSG00000245468	chromatin interactions
ENSG00000200867	chromatin interactions
ENSG00000173011	chromatin interactions
ENSG00000109519	chromatin interactions
KDELC2	miRNA target sites
SPIN4	miRNA target sites
KIAA1274	miRNA target sites
RBM19	miRNA target sites
TUSC2	miRNA target sites
RIOK3	miRNA target sites
ERAP2	miRNA target sites

Extended variants
information (count: 2051 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2051 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11734660	chr4:7093834-7093835	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs535762285	chr4:7093855-7093856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182003425	chr4:7093856-7093857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529908554	chr4:7093915-7093916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548442330	chr4:7093952-7093953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148797950	chr4:7093985-7093986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564444043	chr4:7094024-7094025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139577154	chr4:7094046-7094047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs57163471	chr4:7094048-7094049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529158702	chr4:7094075-7094076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574331750	chr4:7094076-7094077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533126372	chr4:7094079-7094080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186238447	chr4:7094100-7094101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs56917370	chr4:7094102-7094103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs189720492	chr4:7094158-7094159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182069750	chr4:7094208-7094209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs59105243	chr4:7094264-7094265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376852931	chr4:7094287-7094288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186403663	chr4:7094291-7094292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568254183	chr4:7094349-7094350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191311700	chr4:7094378-7094379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371221287	chr4:7094379-7094380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551320920	chr4:7094385-7094386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557501640	chr4:7094389-7094390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146852107	chr4:7094439-7094440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540086558	chr4:7094453-7094454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558173195	chr4:7094455-7094456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576907507	chr4:7094534-7094535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182897946	chr4:7094539-7094540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188799176	chr4:7094606-7094607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs574609842	chr4:7094616-7094617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs547068174	chr4:7094657-7094658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs140681502	chr4:7094661-7094662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs563461616	chr4:7094662-7094663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs190604514	chr4:7094750-7094751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546030529	chr4:7094756-7094757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs183567610	chr4:7094762-7094763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs6446568	chr4:7094764-7094765	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs150969247	chr4:7094765-7094766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs202242716	chr4:7094851-7094852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs7661402	chr4:7094882-7094883	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs550688330	chr4:7094939-7094940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529313771	chr4:7094943-7094944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs140694040	chr4:7094955-7094956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs533162446	chr4:7094960-7094961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs569387891	chr4:7094977-7094978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs530915240	chr4:7094995-7094996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs139723713	chr4:7094996-7094997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs7690647	chr4:7095001-7095002	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs551572736	chr4:7095028-7095029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
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
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
small cell lung cancer	20016488	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
Urothelial carcinoma	21177765	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:870 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7091600-7103600	Weak transcription	Brain Angular Gyrus	brain
2	chr4:7091800-7096400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr4:7092000-7097400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr4:7092000-7103600	Weak transcription	Aorta	Aorta
5	chr4:7092000-7103600	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr4:7092800-7096400	Weak transcription	Fetal Kidney	kidney
7	chr4:7093600-7094600	Weak transcription	Fetal Brain Male	brain
8	chr4:7093600-7096400	Weak transcription	Ovary	ovary
9	chr4:7094600-7095200	Enhancers	Fetal Brain Male	brain
10	chr4:7095200-7097400	Weak transcription	Fetal Brain Male	brain
11	chr4:7096000-7096200	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
12	chr4:7096400-7096600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr4:7096400-7096600	Enhancers	Fetal Kidney	kidney
14	chr4:7096400-7096800	Active TSS	Ovary	ovary
15	chr4:7096600-7096800	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
16	chr4:7096600-7096800	Bivalent Enhancer	K562	blood
17	chr4:7096600-7096800	Flanking Active TSS	NHLF	lung
18	chr4:7096800-7097000	Weak transcription	Ovary	ovary
19	chr4:7096800-7097200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr4:7097000-7098000	Enhancers	Ovary	ovary
21	chr4:7097200-7097400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
22	chr4:7097200-7097600	Enhancers	Spleen	Spleen
23	chr4:7097400-7098200	Enhancers	Fetal Brain Male	brain
24	chr4:7097400-7100000	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr4:7097600-7098000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr4:7097800-7098000	Enhancers	Brain Hippocampus Middle	brain
27	chr4:7098000-7103400	Weak transcription	Ovary	ovary
28	chr4:7098200-7101600	Weak transcription	Brain Substantia Nigra	brain
29	chr4:7098200-7103600	Weak transcription	Fetal Brain Male	brain
30	chr4:7099200-7101600	Weak transcription	Brain Hippocampus Middle	brain
31	chr4:7100000-7103200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr4:7100600-7103800	Weak transcription	HSMMtube	muscle
33	chr4:7101200-7103200	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr4:7101600-7101800	Enhancers	Brain Cingulate Gyrus	brain
35	chr4:7101600-7102000	Enhancers	Brain Hippocampus Middle	brain
36	chr4:7101600-7102000	Enhancers	Brain Substantia Nigra	brain
37	chr4:7101800-7102000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr4:7101800-7102000	Enhancers	Fetal Brain Female	brain
39	chr4:7101800-7103200	Weak transcription	Brain Cingulate Gyrus	brain
40	chr4:7102000-7103000	Weak transcription	Brain Substantia Nigra	brain
41	chr4:7102000-7103200	Weak transcription	Fetal Brain Female	brain
42	chr4:7102000-7103400	Weak transcription	Brain Hippocampus Middle	brain
43	chr4:7102000-7103600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr4:7103000-7103600	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr4:7103000-7103600	Enhancers	Primary B cells from peripheral blood	blood
46	chr4:7103000-7103600	Enhancers	Primary T cells fromperipheralblood	blood
47	chr4:7103000-7103600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr4:7103000-7103600	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr4:7103000-7103600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
50	chr4:7103000-7103600	Enhancers	Primary T killer memory cells from peripheral blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links