Variant report

Variant	esv32642
Chromosome Location	chr3:196118819-196153861
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:228)
CpG islands
(count:62)
Chromatin interactive
region (count:36)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:228 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr3:196139593-196139989	GM12878	blood:	n/a	n/a
2	BCL11A	chr3:196139661-196139935	GM12878	blood:	n/a	n/a
3	BCL11A	chr3:196139587-196139995	GM12878	blood:	n/a	n/a
4	BHLHE40	chr3:196148626-196148866	GM12878	blood:	n/a	n/a
5	BHLHE40	chr3:196126286-196126617	K562	blood:	n/a	n/a
6	BHLHE40	chr3:196139756-196139945	GM12878	blood:	n/a	n/a
7	BRCA1	chr3:196123916-196123958	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr3:196135411-196136212	K562	blood:	n/a	n/a
9	CBX3	chr3:196125654-196126014	K562	blood:	n/a	n/a
10	CBX3	chr3:196135462-196135759	K562	blood:	n/a	n/a
11	CCNT2	chr3:196125554-196125759	K562	blood:	n/a	n/a
12	CEBPB	chr3:196145562-196145826	HepG2	liver:	n/a	n/a
13	CEBPB	chr3:196122476-196122834	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr3:196147267-196147491	K562	blood:	n/a	n/a
15	CEBPB	chr3:196143155-196143330	HepG2	liver:	n/a	n/a
16	CEBPB	chr3:196127076-196127209	HepG2	liver:	n/a	n/a
17	CEBPB	chr3:196143132-196143458	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr3:196122622-196122817	K562	blood:	n/a	n/a
19	CEBPB	chr3:196147365-196147400	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr3:196122491-196122826	IMR90	lung:	n/a	n/a
21	CEBPB	chr3:196122593-196122786	A549	lung:	n/a	n/a
22	CEBPB	chr3:196122576-196122820	HepG2	liver:	n/a	n/a
23	CEBPB	chr3:196122438-196122796	MCF-7	breast:	n/a	n/a
24	CEBPB	chr3:196122387-196122769	A549	lung:	n/a	n/a
25	CEBPB	chr3:196125488-196125638	K562	blood:	n/a	n/a
26	CEBPB	chr3:196143133-196143325	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr3:196143155-196143356	A549	lung:	n/a	n/a
28	CEBPB	chr3:196126597-196127125	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr3:196143118-196143391	IMR90	lung:	n/a	n/a
30	CEBPB	chr3:196143144-196143354	K562	blood:	n/a	n/a
31	CEBPB	chr3:196135813-196136005	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr3:196133810-196133813	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr3:196133141-196133197	GM13976	blood:	n/a	n/a
34	CTCF	chr3:196143760-196143910	SAEC	small airway:	n/a	n/a
35	CTCF	chr3:196148818-196148857	GM13977	blood:	n/a	n/a
36	CTCF	chr3:196149880-196150030	BE2_C	brain:	n/a	n/a
37	CTCF	chr3:196149960-196150110	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr3:196149973-196150071	LNCaP	prostate:	n/a	n/a
39	CTCF	chr3:196128957-196129048	Fibrobl	skin:	n/a	n/a
40	CTCF	chr3:196149940-196150090	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr3:196149960-196150110	BE2_C	brain:	n/a	n/a
42	E2F6	chr3:196135820-196136202	H1-hESC	embryonic stem cell:	n/a	n/a
43	E2F6	chr3:196135750-196136284	H1-hESC	embryonic stem cell:	n/a	n/a
44	EBF1	chr3:196139645-196140082	GM12878	blood:	n/a	n/a
45	EBF1	chr3:196139589-196140184	GM12878	blood:	n/a	n/a
46	EBF1	chr3:196139563-196140038	GM12878	blood:	n/a	n/a
47	EP300	chr3:196126632-196126860	SK-N-SH_RA	brain:	n/a	n/a
48	EP300	chr3:196139612-196140006	GM12878	blood:	n/a	n/a
49	EP300	chr3:196126437-196127060	SK-N-SH	brain:	n/a	n/a
50	EP300	chr3:196139730-196139924	GM12878	blood:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:196134040-196134090	NHDF-neo	bronchial:	n/a
2	chr3:196134040-196134090	NHDF-neo	bronchial:	n/a
3	chr3:196134040-196134090	LNCaP	prostate:	n/a
4	chr3:196134040-196134090	Jurkat	blood:	n/a
5	chr3:196134040-196134090	Caco-2	colon:	n/a
6	chr3:196134040-196134090	A549	lung:	n/a
7	chr3:196134040-196134090	CMK	blood:	n/a
8	chr3:196134040-196134090	H1-hESC	embryonic stem cell:	embryo
9	chr3:196134040-196134090	GM12892	blood:	n/a
10	chr3:196134040-196134090	HIPEpiC	eye:	n/a
11	chr3:196134040-196134090	HNPCEpiC	eye:	n/a
12	chr3:196134040-196134090	HCT-116	colon:	n/a
13	chr3:196134040-196134090	HEK293	kidney:	embryo
14	chr3:196134040-196134090	SAEC	small airway:	n/a
15	chr3:196134040-196134090	HMEC	breast:	n/a
16	chr3:196134040-196134090	SK-N-SH_RA	brain:	n/a
17	chr3:196134040-196134090	MCF-7	breast:	n/a
18	chr3:196134040-196134090	HRPEpiC	eye:	n/a
19	chr3:196134040-196134090	SKMC	muscle:	n/a
20	chr3:196134040-196134090	HepG2	liver:	n/a
21	chr3:196134040-196134090	HRCEpiC	kidney:	n/a
22	chr3:196134040-196134090	AoSMC	blood vessel:	n/a
23	chr3:196134040-196134090	ovcar-3	ovarian:	n/a
24	chr3:196134040-196134090	AG04450	lung:	fetal
25	chr3:196134040-196134090	GM12878	blood:	n/a
26	chr3:196134040-196134090	RPTEC	kidney:	n/a
27	chr3:196134040-196134090	NB4	blood:	n/a
28	chr3:196134040-196134090	HRE	kidney:	n/a
29	chr3:196134040-196134090	GM12891	blood:	n/a
30	chr3:196134040-196134090	PFSK-1	brain:	n/a
31	chr3:196134040-196134090	PANC-1	pancreas:	n/a
32	chr3:196134040-196134090	HCPEpiC	choroid plexus:	n/a
33	chr3:196134040-196134090	MCF10A-Er-Src	breast:	n/a
34	chr3:196134040-196134090	PrEC	prostate:	n/a
35	chr3:196134040-196134090	HAEpiC	amniotic membrane:	n/a
36	chr3:196134040-196134090	HCF	heart:	n/a
37	chr3:196134040-196134090	NHBE	bronchial:	n/a
38	chr3:196134040-196134090	IMR90	lung:	fetal
39	chr3:196134040-196134090	ECC-1	luminal epithelium:	n/a
40	chr3:196134040-196134090	Hela-S3	cervix:	n/a
41	chr3:196134040-196134090	GM06990	blood:	n/a
42	chr3:196134040-196134090	ProgFib	skin:	n/a
43	chr3:196134040-196134090	BJ	skin:	n/a
44	chr3:196134040-196134090	NH-A	brain:	n/a
45	chr3:196134040-196134090	SK-N-MC	brain:	n/a
46	chr3:196134040-196134090	HL-60	blood:	n/a
47	chr3:196134040-196134090	HUVEC	blood vessel:	n/a
48	chr3:196134040-196134090	BE2_C	brain:	n/a
49	chr3:196134040-196134090	AG09309	skin:	n/a
50	chr3:196134040-196134090	T-47D	breast:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:196106180..196108798-chr3:196131015..196133937,2	K562	blood:
2	chr3:196138176..196140569-chr3:196226942..196228528,2	MCF-7	breast:
3	chr3:196135092..196136812-chr3:196230259..196232002,2	MCF-7	breast:
4	chr3:196129528..196131514-chr3:196134157..196136154,2	K562	blood:
5	chr3:196142039..196143861-chr3:196152128..196153766,2	K562	blood:
6	chr3:196133565..196136496-chr3:196147816..196149454,2	K562	blood:
7	chr3:196129090..196131271-chr3:196133908..196136067,2	MCF-7	breast:
8	chr3:196136760..196139527-chr3:196139977..196142790,2	K562	blood:
9	chr3:196044447..196045990-chr3:196139208..196141957,2	MCF-7	breast:
10	chr3:196136134..196138094-chr3:196139731..196142693,2	MCF-7	breast:
11	chr3:196068585..196071026-chr3:196125432..196127097,2	MCF-7	breast:
12	chr3:196145495..196148007-chr3:196148635..196151374,2	MCF-7	breast:
13	chr3:196136760..196139527-chr3:196139977..196142790,2	K562	blood:
14	chr3:196129528..196131514-chr3:196134157..196136154,2	K562	blood:
15	chr3:196133998..196136496-chr3:196146393..196149316,3	K562	blood:
16	chr3:196115479..196118192-chr3:196129291..196130932,2	K562	blood:
17	chr3:196122393..196124913-chr3:196156464..196158992,2	K562	blood:
18	chr3:196133998..196136496-chr3:196146393..196149316,3	K562	blood:
19	chr3:196130460..196132827-chr3:196143494..196145244,2	K562	blood:
20	chr3:196124558..196126207-chr3:196129580..196132524,2	K562	blood:
21	chr3:196103840..196105489-chr3:196133127..196135831,2	K562	blood:
22	chr3:196150524..196154705-chr3:196157628..196161490,4	K562	blood:
23	chr3:196116600..196119227-chr3:196123432..196124939,2	K562	blood:
24	chr3:196130460..196132827-chr3:196143494..196145244,2	K562	blood:
25	chr3:196129090..196131271-chr3:196133908..196136067,2	MCF-7	breast:
26	chr3:196143903..196147509-chr3:196148337..196151296,3	MCF-7	breast:
27	chr3:196141252..196144269-chr3:196156132..196159326,3	K562	blood:
28	chr3:196136134..196138094-chr3:196139731..196142693,2	MCF-7	breast:
29	chr3:196146851..196150238-chr3:196157711..196160603,3	MCF-7	breast:
30	chr3:196065026..196067145-chr3:196151538..196154209,2	K562	blood:
31	chr3:196119980..196121933-chr3:196124713..196127635,2	K562	blood:
32	chr3:196123859..196126007-chr3:196148082..196150188,2	MCF-7	breast:
33	chr3:196141592..196145403-chr3:196157124..196159775,4	MCF-7	breast:
34	chr3:196103840..196105428-chr3:196134331..196136601,2	K562	blood:
35	chr3:196133565..196136496-chr3:196147816..196149454,2	K562	blood:
36	chr3:196119980..196121933-chr3:196124713..196127635,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TM4SF19-1	chr3:196124382-196124649	NONHSAT094331
2	lnc-FBXO45-7	chr3:196150193-196150393	NONHSAT094335
3	lnc-AC069257.9.1-11	chr3:196126782-196127077	NONHSAT094332

No data

Variant related genes	Relation type
RN7SL434P	TF binding region
RN7SL738P	TF binding region
ENSG00000226345	TF binding region
UBXN7	TF binding region
UBXN7-AS1	TF binding region
RNU6-1279P	TF binding region
RN7SL434P	CpG island
RN7SL738P	CpG island
ENSG00000226345	CpG island
UBXN7	CpG island
UBXN7-AS1	CpG island
RNU6-1279P	CpG island
ENSG00000163961	chromatin interactions
ENSG00000163960	chromatin interactions
ENSG00000273331	chromatin interactions
ENSG00000243339	chromatin interactions
ENSG00000225822	chromatin interactions
ENSG00000226345	chromatin interactions
ENSG00000213123	chromatin interactions
ENSG00000272741	chromatin interactions
ENSG00000235897	chromatin interactions
ENSG00000241868	chromatin interactions
ENSG00000206644	chromatin interactions
ENSG00000145107	chromatin interactions
ENSG00000212146	chromatin interactions

Extended variants
information (count: 1397 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1397 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377214001	chr3:196118846-196118847	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs11335716	chr3:196118850-196118851	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs539226946	chr3:196118856-196118857	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs557134989	chr3:196118865-196118866	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs538385226	chr3:196118866-196118867	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs369496809	chr3:196118868-196118869	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs200773493	chr3:196118871-196118872	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs73213958	chr3:196118908-196118909	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs545124763	chr3:196118933-196118934	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs554978986	chr3:196118940-196118941	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs573306439	chr3:196118966-196118967	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs541320243	chr3:196118969-196118970	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs184093412	chr3:196118990-196118991	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs527541767	chr3:196118991-196118992	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs145980527	chr3:196119002-196119003	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs78256600	chr3:196119111-196119112	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs188598064	chr3:196119156-196119157	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs76432815	chr3:196119186-196119187	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs560185183	chr3:196119190-196119191	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs117551338	chr3:196119199-196119200	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs78193934	chr3:196119204-196119205	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs11406393	chr3:196119218-196119219	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs554332839	chr3:196119232-196119233	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs111242924	chr3:196119262-196119263	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7623478	chr3:196119268-196119269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543010563	chr3:196119285-196119286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546843578	chr3:196119292-196119293	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571917314	chr3:196119330-196119331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs146868558	chr3:196119332-196119333	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376213007	chr3:196119336-196119337	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192812117	chr3:196119372-196119373	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183601316	chr3:196119374-196119375	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536726714	chr3:196119408-196119409	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555138852	chr3:196119448-196119449	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547613301	chr3:196119474-196119475	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145689066	chr3:196119511-196119512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188690142	chr3:196119531-196119532	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559158707	chr3:196119552-196119553	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567581023	chr3:196119604-196119605	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191760983	chr3:196119635-196119636	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531532402	chr3:196119653-196119654	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557105142	chr3:196119660-196119661	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575137280	chr3:196119711-196119712	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370834238	chr3:196119721-196119722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs142899207	chr3:196119737-196119738	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548688079	chr3:196119772-196119773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528038256	chr3:196119797-196119798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549914327	chr3:196119840-196119841	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs202013547	chr3:196119879-196119880	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs538700615	chr3:196119887-196119888	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	16397240	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Intracranial aneurysm	16715129	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
Congenital anomalies of the kidney and urinary tract	20299530	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	16760732	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Autism	20970697	CNVD
Developmental delay	18471269	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Uveal melanoma	20484589	CNVD
3q29 microdeletion syndrome	20500065	CNVD
Biliary cancer	20453639	CNVD
3q29 microdeletion syndrome	22283845	CNVD
3q29 microdeletion syndrome	21626679	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1255 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:196073600-196135800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:196083600-196143800	Weak transcription	Psoas Muscle	Psoas
3	chr3:196084600-196131600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr3:196089600-196150000	Weak transcription	Small Intestine	intestine
5	chr3:196094000-196126200	Weak transcription	Colonic Mucosa	Colon
6	chr3:196095600-196144400	Weak transcription	Fetal Heart	heart
7	chr3:196098000-196126800	Weak transcription	Pancreas	Pancrea
8	chr3:196113000-196124600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr3:196113200-196120000	Strong transcription	H1 Cell Line	embryonic stem cell
10	chr3:196113200-196136400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr3:196113400-196119600	Weak transcription	Fetal Brain Male	brain
12	chr3:196115000-196121000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
13	chr3:196115200-196119800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr3:196115200-196120200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr3:196115400-196119200	Strong transcription	Fetal Intestine Large	intestine
16	chr3:196115400-196119400	Strong transcription	Cortex derived primary cultured neurospheres	brain
17	chr3:196115400-196119400	Strong transcription	Thymus	Thymus
18	chr3:196115400-196119800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr3:196115400-196120000	Strong transcription	Primary B cells from cord blood	blood
20	chr3:196115400-196120000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr3:196115400-196120000	Strong transcription	Fetal Muscle Trunk	muscle
22	chr3:196115400-196120200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr3:196115400-196120600	Strong transcription	Primary B cells from peripheral blood	blood
24	chr3:196115400-196120600	Strong transcription	Primary T helper cells PMA-I stimulated	--
25	chr3:196115400-196120600	Strong transcription	Adipose Nuclei	Adipose
26	chr3:196115400-196120800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr3:196115400-196120800	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr3:196115400-196120800	Strong transcription	Primary neutrophils fromperipheralblood	blood
29	chr3:196115400-196120800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr3:196115400-196121000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr3:196115400-196121000	Strong transcription	Fetal Thymus	thymus
32	chr3:196115400-196121600	Strong transcription	Primary T helper cells fromperipheralblood	blood
33	chr3:196115400-196126400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr3:196115400-196127800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr3:196115400-196127800	Strong transcription	Placenta	Placenta
36	chr3:196115400-196127800	Strong transcription	Monocytes-CD14+_RO01746	blood
37	chr3:196115400-196129800	Strong transcription	Primary T cells fromperipheralblood	blood
38	chr3:196115600-196119000	Strong transcription	Primary T killer memory cells from peripheral blood	blood
39	chr3:196115600-196119400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr3:196115600-196120000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr3:196115600-196120400	Strong transcription	Duodenum Smooth Muscle	Duodenum
42	chr3:196115600-196121600	Strong transcription	Dnd41	blood
43	chr3:196115600-196134600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr3:196115800-196119000	Strong transcription	Brain Germinal Matrix	brain
45	chr3:196115800-196119200	Strong transcription	Brain Angular Gyrus	brain
46	chr3:196115800-196120400	Strong transcription	Liver	Liver
47	chr3:196115800-196120400	Strong transcription	Brain Anterior Caudate	brain
48	chr3:196115800-196125400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr3:196116000-196119200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr3:196116000-196119200	Strong transcription	Primary T helper naive cells from peripheral blood	blood

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