Variant report

Variant	esv3331281
Chromosome Location	chr19:43087545-43124628
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr19:43100672-43101041	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr19:43106732-43106880	GM12878	blood:	n/a	n/a
3	BHLHE40	chr19:43110883-43111176	GM12878	blood:	n/a	n/a
4	BHLHE40	chr19:43100628-43100974	K562	blood:	n/a	n/a
5	BHLHE40	chr19:43110839-43111090	K562	blood:	n/a	n/a
6	BRCA1	chr19:43111388-43111484	GM12878	blood:	n/a	n/a
7	CEBPB	chr19:43097919-43098273	A549	lung:	n/a	chr19:43098079-43098092 chr19:43098079-43098090
8	CEBPB	chr19:43098008-43098186	IMR90	lung:	n/a	chr19:43098079-43098092 chr19:43098079-43098090
9	CEBPB	chr19:43110761-43111081	HepG2	liver:	n/a	n/a
10	CEBPB	chr19:43097979-43098209	K562	blood:	n/a	chr19:43098079-43098092 chr19:43098079-43098090
11	CEBPB	chr19:43097951-43098246	HepG2	liver:	n/a	chr19:43098079-43098092 chr19:43098079-43098090
12	CTCF	chr19:43110960-43111110	HEEpiC	esophagus:	n/a	chr19:43111005-43111013 chr19:43111003-43111016 chr19:43111002-43111023 chr19:43111000-43111018 chr19:43111003-43111016 chr19:43111001-43111017
13	CTCF	chr19:43110867-43111116	LNCaP	prostate:	n/a	chr19:43111005-43111013 chr19:43111003-43111016 chr19:43111002-43111023 chr19:43111000-43111018 chr19:43111003-43111016 chr19:43111001-43111017
14	CTCF	chr19:43100120-43100270	GM12864	blood:	n/a	n/a
15	CTCF	chr19:43100700-43100850	WI-38	lung:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
16	CTCF	chr19:43100740-43100890	MCF-7	breast:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
17	CTCF	chr19:43100760-43100910	GM12865	blood:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
18	CTCF	chr19:43110920-43111070	RPTEC	kidney:	n/a	chr19:43111005-43111013 chr19:43111003-43111016 chr19:43111002-43111023 chr19:43111000-43111018 chr19:43111003-43111016 chr19:43111001-43111017
19	CTCF	chr19:43100740-43100890	HMF	breast:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
20	CTCF	chr19:43100740-43100890	BE2_C	brain:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
21	CTCF	chr19:43100780-43100930	WI-38	lung:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
22	CTCF	chr19:43100720-43100870	Hela-S3	cervix:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
23	CTCF	chr19:43100200-43100350	GM12868	blood:	n/a	chr19:43100260-43100273 chr19:43100257-43100275
24	CTCF	chr19:43110920-43111070	GM12878	blood:	n/a	chr19:43111005-43111013 chr19:43111003-43111016 chr19:43111002-43111023 chr19:43111000-43111018 chr19:43111003-43111016 chr19:43111001-43111017
25	CTCF	chr19:43100498-43100598	Fibrobl	skin:	n/a	n/a
26	CTCF	chr19:43100740-43100890	GM12865	blood:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
27	CTCF	chr19:43110920-43111070	AG09319	gingival:	n/a	chr19:43111005-43111013 chr19:43111003-43111016 chr19:43111002-43111023 chr19:43111000-43111018 chr19:43111003-43111016 chr19:43111001-43111017
28	CTCF	chr19:43110701-43110707	Gliobla	brain:	n/a	n/a
29	CTCF	chr19:43101048-43101114	GM10266	blood:	n/a	n/a
30	CTCF	chr19:43100257-43100291	Fibrobl	skin:	n/a	chr19:43100260-43100273 chr19:43100257-43100275
31	CTCF	chr19:43099960-43100110	HEK293	kidney:	n/a	n/a
32	CTCF	chr19:43101077-43101124	Fibrobl	skin:	n/a	n/a
33	CTCF	chr19:43098880-43099030	HepG2	liver:	n/a	n/a
34	CTCF	chr19:43110940-43111090	HL-60	blood:	n/a	chr19:43111005-43111013 chr19:43111003-43111016 chr19:43111002-43111023 chr19:43111000-43111018 chr19:43111003-43111016 chr19:43111001-43111017
35	CTCF	chr19:43100479-43100585	GM12878	blood:	n/a	n/a
36	CTCF	chr19:43100613-43101112	HCT-116	colon:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
37	CTCF	chr19:43100720-43100870	HUVEC	blood vessel:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
38	CTCF	chr19:43100200-43100350	HEK293	kidney:	n/a	chr19:43100260-43100273 chr19:43100257-43100275
39	CTCF	chr19:43110940-43111090	GM12875	blood:	n/a	chr19:43111005-43111013 chr19:43111003-43111016 chr19:43111002-43111023 chr19:43111000-43111018 chr19:43111003-43111016 chr19:43111001-43111017
40	CTCF	chr19:43100633-43100967	H1-hESC	embryonic stem cell:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
41	CTCF	chr19:43110920-43111070	HUVEC	blood vessel:	n/a	chr19:43111005-43111013 chr19:43111003-43111016 chr19:43111002-43111023 chr19:43111000-43111018 chr19:43111003-43111016 chr19:43111001-43111017
42	CTCF	chr19:43100610-43101074	K562	blood:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
43	CTCF	chr19:43100140-43100290	GM12874	blood:	n/a	chr19:43100260-43100273 chr19:43100257-43100275
44	CTCF	chr19:43110380-43110530	GM12866	blood:	n/a	n/a
45	CTCF	chr19:43097820-43097970	SAEC	small airway:	n/a	n/a
46	CTCF	chr19:43100760-43100910	MCF-7	breast:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
47	CTCF	chr19:43100740-43100890	GM12864	blood:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
48	CTCF	chr19:43110520-43110670	HFF	foreskin:	n/a	n/a
49	CTCF	chr19:43110920-43111070	HVMF	connective:	n/a	chr19:43111005-43111013 chr19:43111003-43111016 chr19:43111002-43111023 chr19:43111000-43111018 chr19:43111003-43111016 chr19:43111001-43111017
50	CTCF	chr19:43110920-43111070	HPF	lung:	n/a	chr19:43111005-43111013 chr19:43111003-43111016 chr19:43111002-43111023 chr19:43111000-43111018 chr19:43111003-43111016 chr19:43111001-43111017

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43099795-43099845	BE2_C	brain:	n/a
2	chr19:43099124-43099174	CMK	blood:	n/a
3	chr19:43099046-43099096	PANC-1	pancreas:	n/a
4	chr19:43099845-43099895	ProgFib	skin:	n/a
5	chr19:43099482-43099532	HIPEpiC	eye:	n/a
6	chr19:43099845-43099895	H1-hESC	embryonic stem cell:	embryo
7	chr19:43099795-43099845	HRCEpiC	kidney:	n/a
8	chr19:43099795-43099845	Hepatocyte	liver:	n/a
9	chr19:43099482-43099532	IMR90	lung:	fetal
10	chr19:43099124-43099174	AoSMC	blood vessel:	n/a
11	chr19:43099795-43099845	HPAEpiC	pulmonary alveolar:	n/a
12	chr19:43099795-43099845	GM12878	blood:	n/a
13	chr19:43099795-43099845	CMK	blood:	n/a
14	chr19:43099845-43099895	HNPCEpiC	eye:	n/a
15	chr19:43099046-43099096	Caco-2	colon:	n/a
16	chr19:43099482-43099532	Jurkat	blood:	n/a
17	chr19:43099845-43099895	ovcar-3	ovarian:	n/a
18	chr19:43099124-43099174	ECC-1	luminal epithelium:	n/a
19	chr19:43099845-43099895	NHDF-neo	bronchial:	n/a
20	chr19:43099795-43099845	HEEpiC	esophagus:	n/a
21	chr19:43099795-43099845	AG10803	skin:	n/a
22	chr19:43099482-43099532	PFSK-1	brain:	n/a
23	chr19:43099795-43099845	PFSK-1	brain:	n/a
24	chr19:43099124-43099174	SK-N-MC	brain:	n/a
25	chr19:43099046-43099096	BJ	skin:	n/a
26	chr19:43099124-43099174	K562	blood:	n/a
27	chr19:43099124-43099174	LNCaP	prostate:	n/a
28	chr19:43099482-43099532	HUVEC	blood vessel:	n/a
29	chr19:43099795-43099845	SK-N-MC	brain:	n/a
30	chr19:43099795-43099845	NT2-D1	testis:	n/a
31	chr19:43099795-43099845	NH-A	brain:	n/a
32	chr19:43099795-43099845	SK-N-SH_RA	brain:	n/a
33	chr19:43099845-43099895	AG10803	skin:	n/a
34	chr19:43099482-43099532	SAEC	small airway:	n/a
35	chr19:43099124-43099174	BE2_C	brain:	n/a
36	chr19:43099795-43099845	HEK293	kidney:	embryo
37	chr19:43099124-43099174	HIPEpiC	eye:	n/a
38	chr19:43099124-43099174	GM12892	blood:	n/a
39	chr19:43099046-43099096	T-47D	breast:	n/a
40	chr19:43099845-43099895	PFSK-1	brain:	n/a
41	chr19:43099482-43099532	HL-60	blood:	n/a
42	chr19:43099845-43099895	K562	blood:	n/a
43	chr19:43099046-43099096	HPAEpiC	pulmonary alveolar:	n/a
44	chr19:43099845-43099895	HRCEpiC	kidney:	n/a
45	chr19:43099795-43099845	SAEC	small airway:	n/a
46	chr19:43099482-43099532	ovcar-3	ovarian:	n/a
47	chr19:43099124-43099174	IMR90	lung:	fetal
48	chr19:43099046-43099096	AoSMC	blood vessel:	n/a
49	chr19:43099482-43099532	CMK	blood:	n/a
50	chr19:43099845-43099895	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr19:43110921..43111495-chr19:43166501..43167328,2	MCF-7	breast:
2	chr19:43092830..43095599-chr19:43097248..43100120,2	K562	blood:
3	chr19:42954441..42955205-chr19:43100309..43101289,2	MCF-7	breast:
4	chr19:43110594..43111450-chr19:43197610..43198160,2	MCF-7	breast:
5	chr19:42633464..42636070-chr19:43108015..43110975,2	K562	blood:
6	chr19:43118862..43121094-chr19:43122600..43124613,2	K562	blood:
7	chr19:43070688..43071772-chr19:43100056..43100921,4	MCF-7	breast:
8	chr19:43086009..43087735-chr19:43091658..43093226,2	MCF-7	breast:
9	chr19:43086009..43087735-chr19:43091658..43093226,2	MCF-7	breast:
10	chr19:43070787..43071783-chr19:43100383..43100953,3	MCF-7	breast:
11	chr19:43118862..43121094-chr19:43122600..43124613,2	K562	blood:
12	chr19:43067242..43067993-chr19:43100482..43101078,2	MCF-7	breast:

Variant related genes	Relation type
CEACAM8	TF binding region
CEACAM8	CpG island
ENSG00000124469	chromatin interactions

Extended variants
information (count: 1309 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1309 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567025375	chr19:43087558-43087559	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs535685275	chr19:43087616-43087617	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563059996	chr19:43087660-43087661	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113339180	chr19:43087690-43087691	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555571806	chr19:43087702-43087703	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs371079158	chr19:43087707-43087708	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs35603944	chr19:43087713-43087714	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs34628853	chr19:43087795-43087796	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143755789	chr19:43087797-43087798	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556501317	chr19:43087806-43087807	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs45589137	chr19:43087897-43087898	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs45444792	chr19:43087924-43087925	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552810862	chr19:43087936-43087937	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182361651	chr19:43087949-43087950	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548809873	chr19:43087988-43087989	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542023572	chr19:43088018-43088019	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561910228	chr19:43088102-43088103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530815228	chr19:43088103-43088104	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs35647840	chr19:43088125-43088126	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs186582795	chr19:43088127-43088128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs34786088	chr19:43088136-43088137	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs45606042	chr19:43088184-43088185	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs192645749	chr19:43088201-43088202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529437030	chr19:43088226-43088227	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185750104	chr19:43088253-43088254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569120519	chr19:43088269-43088270	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148121406	chr19:43088276-43088277	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558052233	chr19:43088299-43088300	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs149709504	chr19:43088350-43088351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs56860049	chr19:43088351-43088352	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568291319	chr19:43088355-43088356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs146500700	chr19:43088356-43088357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201374845	chr19:43088380-43088381	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570395320	chr19:43088383-43088384	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs57145552	chr19:43088394-43088395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs10414843	chr19:43088430-43088431	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs570531052	chr19:43088468-43088469	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34599410	chr19:43088502-43088503	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs572847644	chr19:43088510-43088511	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146074163	chr19:43088546-43088547	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562880684	chr19:43088584-43088585	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556439346	chr19:43088672-43088673	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555559340	chr19:43088862-43088863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188666092	chr19:43088876-43088877	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575510225	chr19:43088892-43088893	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556982459	chr19:43088962-43088963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs193163355	chr19:43088974-43088975	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376955363	chr19:43088981-43088982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575534006	chr19:43088990-43088991	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564237047	chr19:43089035-43089036	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43081400-43100600	Weak transcription	Spleen	Spleen
2	chr19:43086200-43088000	Genic enhancers	Primary neutrophils fromperipheralblood	blood
3	chr19:43088000-43092200	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr19:43088400-43088800	Bivalent Enhancer	Primary B cells from cord blood	blood
5	chr19:43088400-43089400	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr19:43088800-43089400	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr19:43090200-43091200	Bivalent Enhancer	Primary B cells from cord blood	blood
8	chr19:43092200-43094400	Genic enhancers	Primary neutrophils fromperipheralblood	blood
9	chr19:43094200-43094400	Enhancers	Primary B cells from cord blood	blood
10	chr19:43094400-43095400	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr19:43094400-43100200	Weak transcription	Primary B cells from cord blood	blood
12	chr19:43095400-43096400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
13	chr19:43096400-43096800	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr19:43096800-43097400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
15	chr19:43096800-43099000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr19:43097400-43097800	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr19:43097800-43099200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
18	chr19:43099200-43099600	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr19:43099600-43100800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
20	chr19:43099800-43100200	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr19:43100200-43100800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr19:43100200-43100800	Enhancers	Primary B cells from cord blood	blood
23	chr19:43100400-43100800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr19:43100400-43101000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
25	chr19:43100400-43101000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
26	chr19:43100400-43101200	Enhancers	Adipose Nuclei	Adipose
27	chr19:43100600-43100800	Bivalent Enhancer	Placenta	Placenta
28	chr19:43100600-43101000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr19:43100600-43101000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr19:43100600-43101000	Enhancers	Right Ventricle	heart
31	chr19:43100600-43101000	Enhancers	Spleen	Spleen
32	chr19:43100600-43101200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
33	chr19:43100600-43101200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr19:43100600-43101200	Enhancers	Brain Cingulate Gyrus	brain
35	chr19:43100600-43101200	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr19:43100600-43101200	Bivalent Enhancer	HepG2	liver
37	chr19:43100800-43101000	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr19:43100800-43101000	Enhancers	Primary T helper naive cells from peripheral blood	blood
39	chr19:43100800-43101000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chr19:43100800-43101200	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr19:43100800-43101200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
42	chr19:43100800-43101200	Bivalent Enhancer	Duodenum Mucosa	Duodenum
43	chr19:43100800-43101200	Enhancers	Esophagus	oesophagus
44	chr19:43100800-43101200	Enhancers	Pancreas	Pancrea
45	chr19:43100800-43101200	Enhancers	K562	blood
46	chr19:43100800-43105800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr19:43101000-43101200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
48	chr19:43101000-43101200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr19:43101000-43101200	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
50	chr19:43101000-43101200	Bivalent Enhancer	Fetal Intestine Small	intestine

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