Variant report

Variant	esv3464811
Chromosome Location	chr4:15646243-15656896
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:798)
CpG islands
(count:305)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:798 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:15655363-15655829	K562	blood:	n/a	n/a
2	ARID3A	chr4:15651601-15651864	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:15656835-15657458	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:15653616-15654052	K562	blood:	n/a	n/a
5	ARID3A	chr4:15656094-15656275	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:15654377-15654628	K562	blood:	n/a	n/a
7	ARID3A	chr4:15656279-15656311	K562	blood:	n/a	n/a
8	ARID3A	chr4:15651500-15652074	K562	blood:	n/a	n/a
9	ARID3A	chr4:15655154-15655813	HepG2	liver:	n/a	n/a
10	ATF1	chr4:15655523-15655892	K562	blood:	n/a	n/a
11	ATF3	chr4:15656703-15657116	A549	lung:	n/a	chr4:15657104-15657113 chr4:15656735-15656744 chr4:15657093-15657113
12	ATF3	chr4:15656876-15657324	GM12878	blood:	n/a	chr4:15657104-15657113 chr4:15657093-15657113
13	BATF	chr4:15651568-15651882	GM12878	blood:	n/a	n/a
14	BATF	chr4:15650261-15650521	GM12878	blood:	n/a	n/a
15	BCL3	chr4:15656616-15657467	A549	lung:	n/a	chr4:15656617-15656630 chr4:15656667-15656680 chr4:15656648-15656661 chr4:15656729-15656742
16	BCL3	chr4:15656632-15657493	A549	lung:	n/a	chr4:15656667-15656680 chr4:15656648-15656661 chr4:15656729-15656742
17	BCL3	chr4:15656555-15657319	GM12878	blood:	n/a	chr4:15656617-15656630 chr4:15656667-15656680 chr4:15656648-15656661 chr4:15656729-15656742
18	BCLAF1	chr4:15651488-15651976	GM12878	blood:	n/a	n/a
19	BCLAF1	chr4:15656310-15657727	GM12878	blood:	n/a	chr4:15656617-15656630 chr4:15656667-15656680 chr4:15656648-15656661 chr4:15656729-15656742
20	BHLHE40	chr4:15656503-15657452	GM12878	blood:	n/a	chr4:15656721-15656737 chr4:15656728-15656744 chr4:15656584-15656600 chr4:15656683-15656699
21	BHLHE40	chr4:15651607-15651867	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:15656620-15657421	K562	blood:	n/a	chr4:15656721-15656737 chr4:15656728-15656744 chr4:15656683-15656699
23	BHLHE40	chr4:15655504-15655947	K562	blood:	n/a	n/a
24	BHLHE40	chr4:15656735-15657421	HepG2	liver:	n/a	n/a
25	CBX3	chr4:15651478-15651959	K562	blood:	n/a	n/a
26	CCNT2	chr4:15656329-15658018	K562	blood:	n/a	chr4:15657746-15657755 chr4:15657603-15657612
27	CEBPB	chr4:15656886-15656890	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr4:15656726-15656865	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr4:15655235-15655857	K562	blood:	n/a	n/a
30	CEBPB	chr4:15656366-15656432	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:15655375-15655797	Hela-S3	cervix:	n/a	n/a
32	CEBPD	chr4:15656785-15657301	HepG2	liver:	n/a	n/a
33	CHD1	chr4:15656349-15657479	GM12878	blood:	n/a	n/a
34	CHD1	chr4:15655942-15656288	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD1	chr4:15656724-15656917	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD1	chr4:15651557-15651847	GM12878	blood:	n/a	n/a
37	CHD1	chr4:15655431-15655567	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr4:15656810-15657465	K562	blood:	n/a	n/a
39	CHD2	chr4:15656741-15657954	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr4:15651548-15651888	GM12878	blood:	n/a	n/a
41	CHD2	chr4:15651584-15651906	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr4:15656607-15657329	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr4:15651579-15651902	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr4:15656832-15657517	GM12878	blood:	n/a	n/a
45	CHD2	chr4:15651532-15651871	K562	blood:	n/a	n/a
46	CHD2	chr4:15651630-15651783	HepG2	liver:	n/a	n/a
47	CREB1	chr4:15656261-15657656	HepG2	liver:	n/a	n/a
48	CREB1	chr4:15656465-15656786	A549	lung:	n/a	n/a
49	CREB1	chr4:15655433-15655959	GM12878	blood:	n/a	n/a
50	CREB1	chr4:15656890-15657202	A549	lung:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:15655683-15655733	HRCEpiC	kidney:	n/a
2	chr4:15656503-15656553	HUVEC	blood vessel:	n/a
3	chr4:15656832-15656882	AoSMC	blood vessel:	n/a
4	chr4:15656874-15656924	SAEC	small airway:	n/a
5	chr4:15656503-15656553	GM12891	blood:	n/a
6	chr4:15655683-15655733	CMK	blood:	n/a
7	chr4:15655683-15655733	AG04450	lung:	fetal
8	chr4:15656832-15656882	HCPEpiC	choroid plexus:	n/a
9	chr4:15655683-15655733	AG09319	gingival:	n/a
10	chr4:15653207-15653257	HCPEpiC	choroid plexus:	n/a
11	chr4:15656874-15656924	CMK	blood:	n/a
12	chr4:15655683-15655733	GM06990	blood:	n/a
13	chr4:15656874-15656924	GM19239	blood:	n/a
14	chr4:15653207-15653257	PFSK-1	brain:	n/a
15	chr4:15655683-15655733	GM19239	blood:	n/a
16	chr4:15656503-15656553	NH-A	brain:	n/a
17	chr4:15656503-15656553	GM12878	blood:	n/a
18	chr4:15656503-15656553	HEEpiC	esophagus:	n/a
19	chr4:15656503-15656553	MCF10A-Er-Src	breast:	n/a
20	chr4:15655683-15655733	NHBE	bronchial:	n/a
21	chr4:15656874-15656924	NHDF-neo	bronchial:	n/a
22	chr4:15656874-15656924	ProgFib	skin:	n/a
23	chr4:15655683-15655733	Hepatocyte	liver:	n/a
24	chr4:15656832-15656882	BE2_C	brain:	n/a
25	chr4:15656874-15656924	HMEC	breast:	n/a
26	chr4:15656503-15656553	HCPEpiC	choroid plexus:	n/a
27	chr4:15656874-15656924	HepG2	liver:	n/a
28	chr4:15653207-15653257	PANC-1	pancreas:	n/a
29	chr4:15656874-15656924	Hepatocyte	liver:	n/a
30	chr4:15656503-15656553	AoSMC	blood vessel:	n/a
31	chr4:15656874-15656924	HNPCEpiC	eye:	n/a
32	chr4:15653207-15653257	NHDF-neo	bronchial:	n/a
33	chr4:15655683-15655733	RPTEC	kidney:	n/a
34	chr4:15656832-15656882	HMEC	breast:	n/a
35	chr4:15653207-15653257	HCM	heart:	n/a
36	chr4:15653207-15653257	LNCaP	prostate:	n/a
37	chr4:15655683-15655733	GM12892	blood:	n/a
38	chr4:15655683-15655733	T-47D	breast:	n/a
39	chr4:15655683-15655733	HNPCEpiC	eye:	n/a
40	chr4:15656832-15656882	T-47D	breast:	n/a
41	chr4:15655683-15655733	AG10803	skin:	n/a
42	chr4:15656874-15656924	U87	brain:	n/a
43	chr4:15656503-15656553	NB4	blood:	n/a
44	chr4:15656503-15656553	AG09319	gingival:	n/a
45	chr4:15655683-15655733	BJ	skin:	n/a
46	chr4:15656503-15656553	AG10803	skin:	n/a
47	chr4:15656832-15656882	SK-N-SH_RA	brain:	n/a
48	chr4:15656503-15656553	Hepatocyte	liver:	n/a
49	chr4:15656503-15656553	HCT-116	colon:	n/a
50	chr4:15656503-15656553	MCF-7	breast:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:15652080..15658606-chr4:15677363..15685579,17	MCF-7	breast:
2	chr21:34601586..34602556-chr4:15656823..15657778,2	NB4	blood:
3	chr4:15650281..15653257-chr4:15654255..15656394,2	K562	blood:
4	chr4:15654963..15657954-chr4:15685988..15688544,3	MCF-7	breast:
5	chr4:15656218..15656918-chr7:45018290..45018877,2	Hela-S3	cervix:
6	chr4:15651703..15660794-chr4:15677607..15686235,25	K562	blood:
7	chr4:15480360..15481040-chr4:15651348..15652082,3	MCF-7	breast:
8	chr4:15650281..15653257-chr4:15654255..15656394,2	K562	blood:
9	chr4:15655595..15658742-chr4:15680185..15687360,10	MCF-7	breast:
10	chr4:15646637..15649068-chr4:15681788..15683669,2	K562	blood:
11	chr4:15650206..15660298-chr4:15677140..15687517,25	K562	blood:
12	chr4:15650347..15653334-chr4:15655350..15658459,4	K562	blood:
13	chr4:15649396..15652390-chr4:15655110..15656784,2	MCF-7	breast:
14	chr4:15544533..15546139-chr4:15654596..15656765,2	K562	blood:
15	chr4:15656159..15658615-chr4:15712805..15714316,2	K562	blood:
16	chr4:15655671..15658131-chr4:15716646..15719360,2	MCF-7	breast:
17	chr4:15654775..15659231-chr4:15659761..15666940,9	K562	blood:
18	chr4:15480731..15481332-chr4:15651437..15652122,2	HCT-116	colon:
19	chr4:15649396..15652390-chr4:15655110..15656784,2	MCF-7	breast:
20	chr4:15652688..15657004-chr4:15659488..15663550,8	K562	blood:
21	chr4:15479691..15482462-chr4:15651754..15655275,3	MCF-7	breast:
22	chr4:15397612..15398426-chr4:15651683..15652206,2	K562	blood:
23	chr4:15002808..15006132-chr4:15656406..15658114,3	K562	blood:
24	chr4:15652202..15654659-chr4:15668639..15670937,2	MCF-7	breast:
25	chr4:15649873..15653235-chr4:15657425..15660766,3	MCF-7	breast:
26	chr4:15480883..15483744-chr4:15651050..15653259,2	MCF-7	breast:
27	chr4:15651951..15654188-chr4:15659620..15662479,2	K562	blood:
28	chr4:15644617..15647033-chr4:15653636..15655308,2	K562	blood:
29	chr4:15479740..15482605-chr4:15655501..15658427,3	MCF-7	breast:
30	chr4:15655590..15657245-chr4:15703796..15706264,2	K562	blood:
31	chr4:15480467..15481583-chr4:15651062..15652266,6	K562	blood:
32	chr12:122235040..122237798-chr4:15655451..15658367,2	MCF-7	breast:

No data

Variant related genes	Relation type
FBXL5	TF binding region
FBXL5	CpG island
ENSG00000137449	chromatin interactions
ENSG00000272849	chromatin interactions
ENSG00000109743	chromatin interactions
ENSG00000136286	chromatin interactions
ENSG00000247624	chromatin interactions
ENSG00000118564	chromatin interactions
ENSG00000237765	chromatin interactions
ENSG00000048342	chromatin interactions
ENSG00000159110	chromatin interactions

Extended variants
information (count: 388 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:388 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17856879	chr4:15646261-15646262	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs186821808	chr4:15646368-15646369	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs373133849	chr4:15646369-15646370	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141926554	chr4:15646493-15646494	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs527265460	chr4:15646529-15646530	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547045502	chr4:15646530-15646531	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs78104228	chr4:15646544-15646545	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs536112639	chr4:15646545-15646546	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549677359	chr4:15646566-15646567	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs530164656	chr4:15646573-15646574	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150669569	chr4:15646583-15646584	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs367951973	chr4:15646592-15646593	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538471877	chr4:15646618-15646619	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs543918952	chr4:15646656-15646657	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs115725900	chr4:15646662-15646663	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs563839034	chr4:15646683-15646684	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs192458619	chr4:15646714-15646715	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs73241180	chr4:15646715-15646716	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs184189079	chr4:15646751-15646752	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs552856444	chr4:15646768-15646769	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs13133213	chr4:15646794-15646795	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs543334815	chr4:15646800-15646801	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs111871922	chr4:15646904-15646905	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs527268339	chr4:15646928-15646929	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs7657257	chr4:15646941-15646942	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs144615375	chr4:15646951-15646952	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs545656570	chr4:15646977-15646978	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs74960141	chr4:15647068-15647069	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs79362497	chr4:15647069-15647070	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs565482436	chr4:15647073-15647074	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs7683000	chr4:15647074-15647075	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs368504855	chr4:15647101-15647102	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs547489324	chr4:15647156-15647157	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs188297266	chr4:15647236-15647237	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs529671640	chr4:15647276-15647277	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs535936255	chr4:15647313-15647314	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs4698407	chr4:15647329-15647330	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs193178457	chr4:15647332-15647333	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs184620835	chr4:15647334-15647335	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs569469218	chr4:15647354-15647355	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs537677451	chr4:15647357-15647358	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs377174172	chr4:15647379-15647380	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs565890124	chr4:15647400-15647401	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs547200478	chr4:15647408-15647409	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs373642432	chr4:15647415-15647416	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs554276429	chr4:15647428-15647429	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs567530079	chr4:15647452-15647453	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs536690695	chr4:15647486-15647487	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs188702667	chr4:15647489-15647490	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs576768187	chr4:15647532-15647533	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	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
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	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
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Breast cancer	22522925	CNVD
Non-small cell lung cancer	21829676	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:787 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:15568400-15655600	Weak transcription	Gastric	stomach
2	chr4:15600800-15653000	Weak transcription	Colonic Mucosa	Colon
3	chr4:15601000-15651600	Weak transcription	Small Intestine	intestine
4	chr4:15602600-15655600	Weak transcription	Pancreas	Pancrea
5	chr4:15605800-15650200	Weak transcription	Stomach Mucosa	stomach
6	chr4:15618600-15651000	Weak transcription	Spleen	Spleen
7	chr4:15622200-15655400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:15627400-15650000	Weak transcription	Fetal Heart	heart
9	chr4:15627400-15651200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr4:15627400-15652400	Weak transcription	Fetal Brain Male	brain
11	chr4:15627600-15646800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr4:15627600-15650200	Weak transcription	Right Ventricle	heart
13	chr4:15628000-15655600	Weak transcription	Lung	lung
14	chr4:15629600-15650400	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr4:15633600-15646400	Strong transcription	Fetal Thymus	thymus
16	chr4:15634600-15646600	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr4:15635000-15647000	Strong transcription	HSMM	muscle
18	chr4:15635600-15646400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr4:15635600-15655600	Weak transcription	Esophagus	oesophagus
20	chr4:15635800-15654800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr4:15636800-15651400	Weak transcription	Hela-S3	cervix
22	chr4:15638600-15648600	Weak transcription	Ovary	ovary
23	chr4:15638600-15651400	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr4:15638800-15647000	Weak transcription	Psoas Muscle	Psoas
25	chr4:15638800-15651600	Weak transcription	NHLF	lung
26	chr4:15638800-15655000	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr4:15639000-15650800	Weak transcription	K562	blood
28	chr4:15640400-15649600	Weak transcription	Brain Hippocampus Middle	brain
29	chr4:15640400-15651600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr4:15641200-15649400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr4:15641200-15649400	Weak transcription	GM12878-XiMat	blood
32	chr4:15641400-15647000	Weak transcription	Primary T cells from cord blood	blood
33	chr4:15641400-15650800	Weak transcription	A549	lung
34	chr4:15641600-15651400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr4:15641800-15649200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
36	chr4:15641800-15649200	Weak transcription	Colon Smooth Muscle	Colon
37	chr4:15641800-15649600	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr4:15641800-15651400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr4:15641800-15653600	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr4:15642000-15650800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr4:15642000-15651400	Weak transcription	HepG2	liver
42	chr4:15642000-15651800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr4:15642000-15652600	Weak transcription	Fetal Brain Female	brain
44	chr4:15642000-15653200	Weak transcription	Fetal Stomach	stomach
45	chr4:15642000-15655200	Weak transcription	Fetal Muscle Trunk	muscle
46	chr4:15642000-15656200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr4:15642400-15647200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr4:15642400-15649000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
49	chr4:15642400-15649200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr4:15642400-15651400	Weak transcription	Primary B cells from cord blood	blood

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