Variant report

Variant	nsv834334
Chromosome Location	chr2:114175740-114338827
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1718)
CpG islands
(count:2931)
Chromatin interactive
region (count:1)
LncRNA
region (count:66)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1718 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:114279097-114279182	K562	blood:	n/a	n/a
2	ARID3A	chr2:114181075-114181226	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:114278614-114278756	K562	blood:	n/a	n/a
4	ATF1	chr2:114309454-114309460	K562	blood:	n/a	n/a
5	ATF1	chr2:114327842-114327962	K562	blood:	n/a	n/a
6	ATF1	chr2:114278555-114278753	K562	blood:	n/a	n/a
7	ATF1	chr2:114195252-114195468	K562	blood:	n/a	n/a
8	ATF3	chr2:114327688-114328010	K562	blood:	n/a	n/a
9	ATF3	chr2:114195215-114195323	K562	blood:	n/a	n/a
10	BATF	chr2:114194949-114195748	GM12878	blood:	n/a	chr2:114195333-114195346
11	BATF	chr2:114217254-114217816	GM12878	blood:	n/a	n/a
12	BATF	chr2:114241890-114242082	GM12878	blood:	n/a	n/a
13	BATF	chr2:114217280-114217821	GM12878	blood:	n/a	n/a
14	BATF	chr2:114188181-114188552	GM12878	blood:	n/a	n/a
15	BATF	chr2:114297909-114298282	GM12878	blood:	n/a	n/a
16	BATF	chr2:114242853-114243066	GM12878	blood:	n/a	n/a
17	BATF	chr2:114285045-114285287	GM12878	blood:	n/a	chr2:114285118-114285128
18	BATF	chr2:114309322-114309698	GM12878	blood:	n/a	chr2:114309606-114309616
19	BATF	chr2:114209720-114209940	GM12878	blood:	n/a	n/a
20	BATF	chr2:114188935-114190118	GM12878	blood:	n/a	chr2:114189910-114189918
21	BATF	chr2:114190291-114190748	GM12878	blood:	n/a	n/a
22	BATF	chr2:114309258-114309659	GM12878	blood:	n/a	chr2:114309606-114309616
23	BATF	chr2:114214368-114214841	GM12878	blood:	n/a	n/a
24	BATF	chr2:114206782-114207175	GM12878	blood:	n/a	n/a
25	BATF	chr2:114251658-114251933	GM12878	blood:	n/a	n/a
26	BATF	chr2:114194968-114195790	GM12878	blood:	n/a	chr2:114195333-114195346
27	BATF	chr2:114221639-114221843	GM12878	blood:	n/a	n/a
28	BATF	chr2:114196059-114196346	GM12878	blood:	n/a	n/a
29	BATF	chr2:114297986-114298283	GM12878	blood:	n/a	n/a
30	BATF	chr2:114179478-114179679	GM12878	blood:	n/a	n/a
31	BATF	chr2:114206835-114207033	GM12878	blood:	n/a	n/a
32	BATF	chr2:114189261-114190171	GM12878	blood:	n/a	chr2:114189910-114189918
33	BATF	chr2:114253690-114253875	GM12878	blood:	n/a	n/a
34	BATF	chr2:114196004-114196344	GM12878	blood:	n/a	n/a
35	BATF	chr2:114284823-114285271	GM12878	blood:	n/a	chr2:114285118-114285128
36	BATF	chr2:114188216-114188558	GM12878	blood:	n/a	n/a
37	BATF	chr2:114190256-114190764	GM12878	blood:	n/a	n/a
38	BATF	chr2:114337655-114337855	GM12878	blood:	n/a	n/a
39	BATF	chr2:114188569-114188750	GM12878	blood:	n/a	n/a
40	BATF	chr2:114217887-114218111	GM12878	blood:	n/a	n/a
41	BATF	chr2:114196999-114197200	GM12878	blood:	n/a	n/a
42	BATF	chr2:114320271-114320529	GM12878	blood:	n/a	chr2:114320367-114320378
43	BATF	chr2:114188894-114189247	GM12878	blood:	n/a	n/a
44	BATF	chr2:114216587-114216848	GM12878	blood:	n/a	n/a
45	BCL11A	chr2:114217254-114217924	GM12878	blood:	n/a	n/a
46	BCL11A	chr2:114309351-114309568	GM12878	blood:	n/a	n/a
47	BCL11A	chr2:114206565-114206813	GM12878	blood:	n/a	n/a
48	BCL11A	chr2:114220336-114220741	GM12878	blood:	n/a	n/a
49	BCL11A	chr2:114189499-114190082	GM12878	blood:	n/a	n/a
50	BCL11A	chr2:114214317-114214657	GM12878	blood:	n/a	n/a

(count:2931 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:114197839-114197889	ProgFib	skin:	n/a
2	chr2:114256392-114256442	LNCaP	prostate:	n/a
3	chr2:114315351-114315401	SK-N-SH_RA	brain:	n/a
4	chr2:114197839-114197889	ProgFib	skin:	n/a
5	chr2:114256392-114256442	LNCaP	prostate:	n/a
6	chr2:114315351-114315401	SK-N-SH_RA	brain:	n/a
7	chr2:114333496-114333546	T-47D	breast:	n/a
8	chr2:114261793-114261843	AG04450	lung:	fetal
9	chr2:114256392-114256442	HRE	kidney:	n/a
10	chr2:114252811-114252861	HPAEpiC	pulmonary alveolar:	n/a
11	chr2:114258120-114258170	BJ	skin:	n/a
12	chr2:114300610-114300660	HRE	kidney:	n/a
13	chr2:114300030-114300080	MCF-7	breast:	n/a
14	chr2:114265743-114265793	NHDF-neo	bronchial:	n/a
15	chr2:114300610-114300660	Caco-2	colon:	n/a
16	chr2:114259669-114259719	K562	blood:	n/a
17	chr2:114259244-114259294	CMK	blood:	n/a
18	chr2:114256406-114256456	PFSK-1	brain:	n/a
19	chr2:114311462-114311512	GM06990	blood:	n/a
20	chr2:114300610-114300660	Hela-S3	cervix:	n/a
21	chr2:114195528-114195578	GM06990	blood:	n/a
22	chr2:114256454-114256504	GM06990	blood:	n/a
23	chr2:114265743-114265793	ECC-1	luminal epithelium:	n/a
24	chr2:114256781-114256831	GM12891	blood:	n/a
25	chr2:114260142-114260192	AG04449	skin:	fetal
26	chr2:114334065-114334115	HepG2	liver:	n/a
27	chr2:114265743-114265793	GM12891	blood:	n/a
28	chr2:114269216-114269266	NHDF-neo	bronchial:	n/a
29	chr2:114261979-114262029	HMEC	breast:	n/a
30	chr2:114303932-114303982	LNCaP	prostate:	n/a
31	chr2:114257348-114257398	AG09309	skin:	n/a
32	chr2:114256673-114256723	Hela-S3	cervix:	n/a
33	chr2:114269216-114269266	GM12878	blood:	n/a
34	chr2:114326007-114326057	HMEC	breast:	n/a
35	chr2:114269216-114269266	AG04449	skin:	fetal
36	chr2:114261793-114261843	Caco-2	colon:	n/a
37	chr2:114312189-114312239	U87	brain:	n/a
38	chr2:114260766-114260816	HCT-116	colon:	n/a
39	chr2:114197839-114197889	T-47D	breast:	n/a
40	chr2:114196058-114196108	AG10803	skin:	n/a
41	chr2:114261369-114261419	Caco-2	colon:	n/a
42	chr2:114261793-114261843	CMK	blood:	n/a
43	chr2:114194541-114194591	NHDF-neo	bronchial:	n/a
44	chr2:114261793-114261843	Jurkat	blood:	n/a
45	chr2:114256406-114256456	SK-N-MC	brain:	n/a
46	chr2:114252811-114252861	HRE	kidney:	n/a
47	chr2:114194541-114194591	AG09319	gingival:	n/a
48	chr2:114260766-114260816	NH-A	brain:	n/a
49	chr2:114311462-114311512	PFSK-1	brain:	n/a
50	chr2:114326007-114326057	PFSK-1	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:114284812..114285348-chr2:114457736..114458446,2	MCF-7	breast:

(count:66 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC016745.1-6	chr2:114305096-114305475	NONHSAT073799
2	lnc-FOXD4L1-1	chr2:114270040-114270171	XLOC_001631
3	lnc-FOXD4L1-1	chr2:114261556-114261635	XLOC_001631
4	lnc-FOXD4L1-1	chr2:114269931-114271125	XLOC_001631
5	lnc-FOXD4L1-1	chr2:114261620-114262184	NONHSAT073783
6	lnc-AC016745.1-1	chr2:114298727-114298783	ENSG00000231943
7	lnc-AC016745.1-6	chr2:114335509-114335609	l_1930_chr2:114303057-114317403_testes
8	lnc-CBWD2-2	chr2:114190177-114193619	ENSG00000272563.1
9	lnc-RABL2A-2	chr2:114334959-114335319	ENSG00000226516.3
10	lnc-FOXD4L1-1	chr2:114261833-114262184	XLOC_001631
11	lnc-AC016745.1-1	chr2:114300124-114300213	ENSG00000231943
12	lnc-RABL2A-2	chr2:114335559-114335763	XLOC_001632
13	lnc-FOXD4L1-1	chr2:114265430-114265842	XLOC_001631
14	lnc-RABL2A-2	chr2:114335866-114336429	ENSG00000226516.3
15	lnc-AC016745.1-1	chr2:114286497-114286679	ENSG00000231943
16	lnc-AC016745.1-6	chr2:114303058-114303584	l_1930_chr2:114303057-114317403_testes
17	lnc-AC016745.1-1	chr2:114297629-114298046	ENSG00000231943
18	lnc-AC016745.1-1	chr2:114297633-114298046	ENSG00000231943
19	lnc-AC016745.1-6	chr2:114305577-114305635	l_1930_chr2:114303057-114317403_testes
20	lnc-AC016745.1-6	chr2:114304899-114305166	NONHSAT073798
21	lnc-AC016745.1-6	chr2:114305577-114305774	NONHSAT073799
22	lnc-AC016745.1-1	chr2:114286224-114286679	ENSG00000231943
23	lnc-RABL2A-2	chr2:114335866-114336428	XLOC_001632
24	lnc-AC016745.1-1	chr2:114285145-114285229	ENSG00000231943
25	lnc-CBWD2-1	chr2:114182072-114182152	ENSG00000234997.1
26	lnc-AC016745.1-4	chr2:114186646-114186941	expReg_chr2_8628_-
27	lnc-FOXD4L1-1	chr2:114261182-114261242	XLOC_001631
28	lnc-FOXD4L1-1	chr2:114271015-114271076	XLOC_001631
29	lnc-FOXD4L1-1	chr2:114261833-114261941	XLOC_001631
30	lnc-AC016745.1-1	chr2:114300124-114300242	ENSG00000231943
31	lnc-AC016745.1-1	chr2:114292137-114292293	ENSG00000231943
32	lnc-AC016745.1-6	chr2:114303437-114303584	NONHSAT073798
33	lnc-RABL2A-2	chr2:114334959-114335319	ENSG00000226516.3
34	lnc-RABL2A-2	chr2:114336158-114336486	XLOC_001632
35	lnc-AC016745.1-6	chr2:114305577-114305632	NONHSAT073800
36	lnc-FOXD4L1-1	chr2:114261181-114261242	NONHSAT073783
37	lnc-RABL2A-2	chr2:114335559-114335763	ENSG00000226516
38	lnc-AC016745.1-1	chr2:114300124-114300249	ENSG00000231943
39	lnc-FOXD4L1-1	chr2:114271088-114271125	XLOC_001631
40	lnc-AC016745.1-1	chr2:114300124-114300235	ENSG00000231943
41	lnc-FOXD4L1-1	chr2:114271015-114271125	XLOC_001631
42	lnc-RABL2A-2	chr2:114335559-114336429	ENSG00000226516.3
43	lnc-RABL2A-2	chr2:114335192-114335319	ENSG00000226516
44	lnc-FOXD4L1-1	chr2:114272561-114272896	XLOC_001631
45	lnc-AC016745.1-1	chr2:114293384-114293576	ENSG00000231943
46	lnc-AC016745.1-6	chr2:114305235-114305475	NONHSAT073800
47	lnc-FOXD4L1-1	chr2:114272561-114273062	XLOC_001631
48	lnc-FOXD4L1-1	chr2:114261680-114261941	XLOC_001631
49	lnc-RABL2A-2	chr2:114334959-114335319	XLOC_001632
50	lnc-RABL2A-2	chr2:114335866-114336353	ENSG00000226516

No data

Variant related genes	Relation type
ENSG00000238091	TF binding region
ENSG00000225398	TF binding region
CBWD2	TF binding region
WASH2P	TF binding region
ENSG00000272563	TF binding region
FOXD4L1	TF binding region
ENSG00000234997	TF binding region
ENSG00000234148	TF binding region
FAM138B	TF binding region
ENSG00000231943	TF binding region
ENSG00000238091	CpG island
ENSG00000225398	CpG island
CBWD2	CpG island
WASH2P	CpG island
ENSG00000272563	CpG island
FOXD4L1	CpG island
ENSG00000234997	CpG island
ENSG00000234148	CpG island
FAM138B	CpG island
ENSG00000231943	CpG island
GZF1	miRNA target sites
SIAH1	miRNA target sites
SMURF1	miRNA target sites
C11orf41	miRNA target sites
C11orf54	miRNA target sites
C10orf88	miRNA target sites
CUL2	miRNA target sites
H2AFX	miRNA target sites

Extended variants
information (count: 3417 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:3417 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369936189	chr2:114175745-114175746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs62160000	chr2:114177936-114177937	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs2441394	chr2:114177945-114177946	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs55700492	chr2:114177951-114177952	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs200904247	chr2:114177965-114177966	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs530575033	chr2:114178019-114178020	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs550705302	chr2:114178080-114178081	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs60370771	chr2:114178096-114178097	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs62160001	chr2:114178129-114178130	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs371403752	chr2:114178143-114178144	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs370829075	chr2:114178154-114178155	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs2757955	chr2:114178183-114178184	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs368728987	chr2:114178254-114178255	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs113713933	chr2:114178317-114178318	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs112947210	chr2:114178320-114178321	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs55868334	chr2:114178388-114178389	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs55907427	chr2:114178398-114178399	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs56277096	chr2:114178407-114178408	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs28735465	chr2:114178413-114178414	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs200201234	chr2:114178460-114178461	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs201778990	chr2:114178489-114178490	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs112571712	chr2:114178554-114178555	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs577362668	chr2:114179051-114179052	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs55963171	chr2:114179202-114179203	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs201638973	chr2:114179221-114179222	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs546105766	chr2:114179245-114179246	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs200365521	chr2:114179264-114179265	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs553549896	chr2:114179293-114179294	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs573552416	chr2:114179338-114179339	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs202046881	chr2:114179343-114179344	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs542545901	chr2:114179421-114179422	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs561628497	chr2:114179445-114179446	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs191858180	chr2:114179489-114179490	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs3895280	chr2:114179531-114179532	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs544293951	chr2:114179544-114179545	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs184055485	chr2:114179552-114179553	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs533134559	chr2:114179624-114179625	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs546444194	chr2:114179675-114179676	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs201433805	chr2:114180070-114180071	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs60229484	chr2:114180107-114180108	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs567553728	chr2:114180170-114180171	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs553246428	chr2:114180194-114180195	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs556143252	chr2:114180432-114180433	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs575291278	chr2:114180498-114180499	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs186632703	chr2:114180700-114180701	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs1191643	chr2:114180704-114180705	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs372320229	chr2:114180727-114180728	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs529092247	chr2:114180739-114180740	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs548860151	chr2:114180828-114180829	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs190006991	chr2:114180874-114180875	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1034 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:114174200-114175800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:114181000-114181400	Enhancers	HepG2	liver
3	chr2:114187000-114191400	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr2:114187400-114187600	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr2:114187400-114187800	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr2:114187800-114188200	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr2:114188200-114189800	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr2:114188400-114188800	Enhancers	Primary B cells from peripheral blood	blood
9	chr2:114188400-114189800	Active TSS	Monocytes-CD14+_RO01746	blood
10	chr2:114188600-114189000	Active TSS	GM12878-XiMat	blood
11	chr2:114188800-114189000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr2:114188800-114189800	Weak transcription	Primary B cells from peripheral blood	blood
13	chr2:114188800-114191200	Enhancers	Primary B cells from cord blood	blood
14	chr2:114189000-114189600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr2:114189000-114189800	Weak transcription	GM12878-XiMat	blood
16	chr2:114189400-114190200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr2:114189600-114190200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr2:114189800-114190000	Active TSS	GM12878-XiMat	blood
19	chr2:114189800-114190200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
20	chr2:114189800-114190200	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr2:114189800-114190200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
22	chr2:114189800-114191400	Enhancers	Primary B cells from peripheral blood	blood
23	chr2:114190000-114190200	Flanking Active TSS	GM12878-XiMat	blood
24	chr2:114190200-114190400	Active TSS	Primary neutrophils fromperipheralblood	blood
25	chr2:114190200-114190400	Enhancers	GM12878-XiMat	blood
26	chr2:114190200-114191000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr2:114190200-114191200	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr2:114190200-114194600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr2:114190200-114194600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr2:114190400-114190800	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr2:114190400-114190800	Weak transcription	GM12878-XiMat	blood
32	chr2:114190800-114191400	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr2:114190800-114191400	Enhancers	GM12878-XiMat	blood
34	chr2:114191000-114191200	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr2:114191200-114194200	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr2:114191200-114195000	Weak transcription	Primary B cells from cord blood	blood
37	chr2:114191200-114195000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr2:114191400-114194200	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr2:114191400-114194600	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr2:114191400-114194600	Weak transcription	Primary B cells from peripheral blood	blood
41	chr2:114191400-114195400	Weak transcription	GM12878-XiMat	blood
42	chr2:114194200-114195000	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr2:114194200-114195000	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr2:114194600-114194800	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr2:114194600-114194800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr2:114194600-114194800	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr2:114194600-114195000	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr2:114194600-114195000	Enhancers	Primary B cells from peripheral blood	blood
49	chr2:114194600-114195000	Enhancers	Primary T cells fromperipheralblood	blood
50	chr2:114194600-114195000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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