Variant report

Variant	nsv522792
Chromosome Location	chr4:106895964-106982793
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:445)
CpG islands
(count:244)
Chromatin interactive
region (count:26)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:445 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:106918194-106918362	K562	blood:	n/a	n/a
2	ARID3A	chr4:106919325-106919812	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:106957839-106958696	HepG2	liver:	n/a	n/a
4	BACH1	chr4:106918106-106918270	K562	blood:	n/a	n/a
5	BATF	chr4:106978142-106978422	GM12878	blood:	n/a	n/a
6	BATF	chr4:106978117-106978395	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:106918002-106918365	K562	blood:	n/a	n/a
8	BHLHE40	chr4:106958078-106958402	HepG2	liver:	n/a	n/a
9	BHLHE40	chr4:106919292-106919643	HepG2	liver:	n/a	n/a
10	CBX3	chr4:106932620-106932895	K562	blood:	n/a	n/a
11	CBX3	chr4:106934269-106934561	K562	blood:	n/a	n/a
12	CBX3	chr4:106932657-106932841	K562	blood:	n/a	n/a
13	CBX3	chr4:106917935-106918367	K562	blood:	n/a	n/a
14	CBX3	chr4:106911921-106912690	HCT-116	colon:	n/a	n/a
15	CBX3	chr4:106934273-106934527	K562	blood:	n/a	n/a
16	CCNT2	chr4:106898195-106898398	K562	blood:	n/a	n/a
17	CCNT2	chr4:106918060-106918280	K562	blood:	n/a	n/a
18	CEBPB	chr4:106928473-106928631	MCF-7	breast:	n/a	n/a
19	CEBPB	chr4:106921250-106921575	HepG2	liver:	n/a	chr4:106921430-106921441
20	CEBPB	chr4:106898098-106898280	A549	lung:	n/a	chr4:106898192-106898203
21	CEBPB	chr4:106898045-106898360	HepG2	liver:	n/a	chr4:106898192-106898203
22	CEBPB	chr4:106921275-106921518	K562	blood:	n/a	chr4:106921430-106921441
23	CEBPB	chr4:106923614-106923626	K562	blood:	n/a	n/a
24	CEBPB	chr4:106928517-106928733	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:106965746-106965951	A549	lung:	n/a	chr4:106965872-106965883
26	CEBPB	chr4:106959329-106959333	K562	blood:	n/a	n/a
27	CEBPB	chr4:106921258-106921522	A549	lung:	n/a	chr4:106921430-106921441
28	CEBPB	chr4:106958067-106958754	HepG2	liver:	n/a	chr4:106958600-106958611 chr4:106958600-106958613 chr4:106958600-106958613
29	CEBPB	chr4:106965737-106965971	ECC-1	luminal epithelium:	n/a	chr4:106965872-106965883
30	CEBPB	chr4:106898025-106898331	IMR90	lung:	n/a	chr4:106898192-106898203
31	CEBPB	chr4:106965724-106966028	HepG2	liver:	n/a	chr4:106965872-106965883
32	CEBPB	chr4:106897982-106898384	K562	blood:	n/a	chr4:106898192-106898203
33	CEBPB	chr4:106965726-106966055	K562	blood:	n/a	chr4:106965872-106965883
34	CEBPB	chr4:106965718-106966045	IMR90	lung:	n/a	chr4:106965872-106965883
35	CEBPB	chr4:106923446-106923621	HepG2	liver:	n/a	chr4:106923558-106923569
36	CEBPB	chr4:106898144-106898258	H1-hESC	embryonic stem cell:	n/a	chr4:106898192-106898203
37	CEBPB	chr4:106965757-106966048	Hela-S3	cervix:	n/a	chr4:106965872-106965883
38	CEBPB	chr4:106969776-106970053	IMR90	lung:	n/a	n/a
39	CEBPB	chr4:106898008-106898414	K562	blood:	n/a	chr4:106898192-106898203
40	CEBPB	chr4:106971713-106971951	HepG2	liver:	n/a	chr4:106971883-106971894 chr4:106971883-106971896 chr4:106971885-106971894 chr4:106971883-106971896 chr4:106971885-106971896
41	CEBPB	chr4:106898077-106898248	K562	blood:	n/a	chr4:106898192-106898203
42	CEBPD	chr4:106918046-106918493	K562	blood:	n/a	n/a
43	CEBPD	chr4:106917969-106918398	K562	blood:	n/a	n/a
44	CHD2	chr4:106918232-106918291	K562	blood:	n/a	n/a
45	CTCF	chr4:106913020-106913170	HepG2	liver:	n/a	n/a
46	CTCF	chr4:106970200-106970350	AG09319	gingival:	n/a	n/a
47	CTCF	chr4:106953800-106953950	HepG2	liver:	n/a	n/a
48	CTCF	chr4:106912960-106913110	HAc	cerebellar:	n/a	n/a
49	CTCF	chr4:106913040-106913190	BE2_C	brain:	n/a	n/a
50	CTCF	chr4:106913007-106913181	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	chr4:106957718-106957768	HEEpiC	esophagus:	n/a
2	chr4:106957718-106957768	HRE	kidney:	n/a
3	chr4:106967367-106967417	IMR90	lung:	fetal
4	chr4:106978683-106978733	AoSMC	blood vessel:	n/a
5	chr4:106967367-106967417	ECC-1	luminal epithelium:	n/a
6	chr4:106957718-106957768	ECC-1	luminal epithelium:	n/a
7	chr4:106969512-106969562	HIPEpiC	eye:	n/a
8	chr4:106978683-106978733	NT2-D1	testis:	n/a
9	chr4:106978683-106978733	AG09319	gingival:	n/a
10	chr4:106978683-106978733	HUVEC	blood vessel:	n/a
11	chr4:106967367-106967417	HEEpiC	esophagus:	n/a
12	chr4:106969512-106969562	HPAEpiC	pulmonary alveolar:	n/a
13	chr4:106969512-106969562	MCF-7	breast:	n/a
14	chr4:106957718-106957768	SK-N-SH	brain:	n/a
15	chr4:106957718-106957768	ovcar-3	ovarian:	n/a
16	chr4:106978683-106978733	Hepatocyte	liver:	n/a
17	chr4:106957718-106957768	NB4	blood:	n/a
18	chr4:106978683-106978733	AG10803	skin:	n/a
19	chr4:106967367-106967417	A549	lung:	n/a
20	chr4:106957718-106957768	Hepatocyte	liver:	n/a
21	chr4:106978683-106978733	PFSK-1	brain:	n/a
22	chr4:106957718-106957768	HRPEpiC	eye:	n/a
23	chr4:106978683-106978733	SK-N-SH	brain:	n/a
24	chr4:106967367-106967417	Caco-2	colon:	n/a
25	chr4:106969512-106969562	SKMC	muscle:	n/a
26	chr4:106967367-106967417	HCT-116	colon:	n/a
27	chr4:106978683-106978733	AG09309	skin:	n/a
28	chr4:106978683-106978733	HCM	heart:	n/a
29	chr4:106969512-106969562	NT2-D1	testis:	n/a
30	chr4:106978683-106978733	CMK	blood:	n/a
31	chr4:106969512-106969562	HRE	kidney:	n/a
32	chr4:106967367-106967417	HNPCEpiC	eye:	n/a
33	chr4:106957718-106957768	AoSMC	blood vessel:	n/a
34	chr4:106957718-106957768	NH-A	brain:	n/a
35	chr4:106957718-106957768	NT2-D1	testis:	n/a
36	chr4:106957718-106957768	AG09309	skin:	n/a
37	chr4:106969512-106969562	IMR90	lung:	fetal
38	chr4:106969512-106969562	GM06990	blood:	n/a
39	chr4:106967367-106967417	HAEpiC	amniotic membrane:	n/a
40	chr4:106978683-106978733	NHBE	bronchial:	n/a
41	chr4:106969512-106969562	HCM	heart:	n/a
42	chr4:106969512-106969562	A549	lung:	n/a
43	chr4:106967367-106967417	PFSK-1	brain:	n/a
44	chr4:106967367-106967417	HRCEpiC	kidney:	n/a
45	chr4:106957718-106957768	HNPCEpiC	eye:	n/a
46	chr4:106957718-106957768	SAEC	small airway:	n/a
47	chr4:106967367-106967417	GM19239	blood:	n/a
48	chr4:106957718-106957768	NHBE	bronchial:	n/a
49	chr4:106969512-106969562	Jurkat	blood:	n/a
50	chr4:106967367-106967417	Jurkat	blood:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:106873748..106874335-chr4:106920222..106921054,2	MCF-7	breast:
2	chr4:106952681..106954677-chr4:106971571..106974056,2	K562	blood:
3	chr4:106925210..106927104-chr4:106934407..106935960,2	MCF-7	breast:
4	chr4:106899986..106902171-chr4:106913002..106915324,2	K562	blood:
5	chr4:106969485..106971896-chr4:106985535..106988027,2	K562	blood:
6	chr4:106893048..106895457-chr4:106896581..106900704,4	K562	blood:
7	chr4:106933880..106935775-chr4:106939732..106941383,2	K562	blood:
8	chr4:106630458..106633025-chr4:106894653..106897415,2	MCF-7	breast:
9	chr4:106816125..106818142-chr4:106978874..106981523,2	MCF-7	breast:
10	chr14:24562244..24564068-chr4:106897955..106900240,2	MCF-7	breast:
11	chr4:106933880..106935775-chr4:106939732..106941383,2	K562	blood:
12	chr4:106915060..106916769-chr4:106919468..106922442,2	MCF-7	breast:
13	chr4:106899986..106902171-chr4:106913002..106915324,2	K562	blood:
14	chr4:106915060..106916769-chr4:106919468..106922442,2	MCF-7	breast:
15	chr4:106925210..106927104-chr4:106934407..106935960,2	MCF-7	breast:
16	chr4:106818843..106821776-chr4:106981675..106983707,2	MCF-7	breast:
17	chr4:106934510..106937161-chr4:106937686..106939688,2	K562	blood:
18	chr4:106909185..106911956-chr4:106914029..106916741,2	K562	blood:
19	chr4:106954975..106957193-chr4:106960681..106963190,2	MCF-7	breast:
20	chr4:106978527..106980178-chr4:106980635..106982411,2	MCF-7	breast:
21	chr4:106978527..106980178-chr4:106980635..106982411,2	MCF-7	breast:
22	chr4:106934510..106937161-chr4:106937686..106939688,2	K562	blood:
23	chr4:106954975..106957193-chr4:106960681..106963190,2	MCF-7	breast:
24	chr4:106973955..106976797-chr4:106984969..106987253,2	K562	blood:
25	chr4:106909185..106911956-chr4:106914029..106916741,2	K562	blood:
26	chr4:106952681..106954677-chr4:106971571..106974056,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TBCK-1	chr4:106924474-106925113	XLOC_004040
2	lnc-TBCK-1	chr4:106940966-106943635	XLOC_004040
3	lnc-TBCK-4	chr4:106962789-106964536	NONHSAT097701
4	lnc-TBCK-1	chr4:106939826-106939916	XLOC_004040
5	lnc-TBCK-1	chr4:106935345-106935469	XLOC_004040

No data

Variant related genes	Relation type
ENSG00000249635	TF binding region
ENSG00000249635	CpG island
ENSG00000138780	chromatin interactions
ENSG00000253989	chromatin interactions
ENSG00000100889	chromatin interactions
ENSG00000168743	chromatin interactions
ENSG00000138785	chromatin interactions

Extended variants
information (count: 2696 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:2696 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10001634	chr4:106895964-106895965	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187551818	chr4:106895973-106895974	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs558531333	chr4:106895982-106895983	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs574488619	chr4:106895987-106895988	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs141921368	chr4:106896006-106896007	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs192192351	chr4:106896013-106896014	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs560679308	chr4:106896046-106896047	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs33951610	chr4:106896053-106896054	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs574185047	chr4:106896067-106896068	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs540516622	chr4:106896097-106896098	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs572495043	chr4:106896116-106896117	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs543121138	chr4:106896126-106896127	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs150258031	chr4:106896144-106896145	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs560740999	chr4:106896153-106896154	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs185038194	chr4:106896265-106896266	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs28735827	chr4:106896272-106896273	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs138937795	chr4:106896276-106896277	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs149439371	chr4:106896287-106896288	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs28488638	chr4:106896302-106896303	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs568612361	chr4:106896455-106896456	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs145932537	chr4:106896461-106896462	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs376157933	chr4:106896462-106896463	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs538907942	chr4:106896503-106896504	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs566671709	chr4:106896525-106896526	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs10002265	chr4:106896602-106896603	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs111931734	chr4:106896679-106896680	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs3974417	chr4:106896680-106896681	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs189983933	chr4:106896695-106896696	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs199823113	chr4:106896711-106896712	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs200305784	chr4:106896712-106896713	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs371621162	chr4:106896756-106896757	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs575175696	chr4:106896791-106896792	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs139797117	chr4:106896798-106896799	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs10025012	chr4:106896810-106896811	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs374443374	chr4:106896866-106896867	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs574047024	chr4:106896890-106896891	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs181264744	chr4:106896908-106896909	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs141546561	chr4:106896991-106896992	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs146200728	chr4:106896993-106896994	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs546056072	chr4:106897033-106897034	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs17036415	chr4:106897054-106897055	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs148429924	chr4:106897069-106897070	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs548652235	chr4:106897106-106897107	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs28602429	chr4:106897179-106897180	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs184645153	chr4:106897208-106897209	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs557174069	chr4:106897210-106897211	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs13111040	chr4:106897229-106897230	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs547886322	chr4:106897291-106897292	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs188317009	chr4:106897295-106897296	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs566245513	chr4:106897296-106897297	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
myeloid cancer	21057493	CNVD
Cognitive impairment	21505072	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:505 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:106885400-106909800	Weak transcription	Aorta	Aorta
2	chr4:106891000-106898600	Weak transcription	Fetal Intestine Large	intestine
3	chr4:106891800-106897800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr4:106892400-106900000	Weak transcription	HSMMtube	muscle
5	chr4:106893200-106897200	Weak transcription	Fetal Intestine Small	intestine
6	chr4:106897200-106897400	Enhancers	Fetal Intestine Small	intestine
7	chr4:106897800-106899400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:106897800-106900600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr4:106897800-106901400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr4:106898400-106899000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr4:106898400-106899000	Enhancers	Fetal Heart	heart
12	chr4:106898600-106899000	Enhancers	Fetal Intestine Large	intestine
13	chr4:106898800-106899000	Enhancers	Adipose Nuclei	Adipose
14	chr4:106899000-106900000	Weak transcription	Adipose Nuclei	Adipose
15	chr4:106899400-106899600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr4:106899600-106900000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr4:106899600-106900600	Enhancers	NHEK	skin
18	chr4:106900000-106900400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr4:106900000-106900400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr4:106900000-106900400	Enhancers	Adipose Nuclei	Adipose
21	chr4:106900000-106900600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr4:106900000-106900800	Enhancers	HUVEC	blood vessel
23	chr4:106900000-106901000	Enhancers	HSMMtube	muscle
24	chr4:106900000-106901000	Enhancers	Osteobl	bone
25	chr4:106900200-106900800	Enhancers	NH-A	brain
26	chr4:106900200-106901000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr4:106900200-106901000	Enhancers	Muscle Satellite Cultured Cells	--
28	chr4:106900200-106901000	Enhancers	HSMM	muscle
29	chr4:106900200-106901400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr4:106900200-106901400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr4:106900200-106901400	Enhancers	NHDF-Ad	bronchial
32	chr4:106900600-106901400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr4:106906000-106906200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
34	chr4:106907800-106925000	Weak transcription	Pancreas	Pancrea
35	chr4:106909600-106911400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr4:106909800-106910000	Enhancers	Psoas Muscle	Psoas
37	chr4:106909800-106910200	Enhancers	Left Ventricle	heart
38	chr4:106909800-106913000	Enhancers	Aorta	Aorta
39	chr4:106909800-106913200	Enhancers	HUVEC	blood vessel
40	chr4:106910000-106910200	Enhancers	Lung	lung
41	chr4:106910000-106910800	Weak transcription	Psoas Muscle	Psoas
42	chr4:106910000-106913200	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr4:106910000-106913400	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr4:106910200-106910400	Weak transcription	Fetal Muscle Leg	muscle
45	chr4:106910200-106911400	Weak transcription	Left Ventricle	heart
46	chr4:106910400-106912800	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr4:106910400-106913400	Enhancers	Fetal Muscle Leg	muscle
48	chr4:106910600-106913200	Enhancers	Muscle Satellite Cultured Cells	--
49	chr4:106910600-106913200	Enhancers	Fetal Heart	heart
50	chr4:106910600-106913200	Enhancers	Fetal Stomach	stomach

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