Variant report

Variant	esv2755193
Chromosome Location	chr2:113467769-113478769
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:167)
CpG islands
(count:61)
Chromatin interactive
region (count:39)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:167 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:113470854-113471064	K562	blood:	n/a	n/a
2	ARID3A	chr2:113470816-113471130	HepG2	liver:	n/a	n/a
3	ATF1	chr2:113476270-113476404	K562	blood:	n/a	n/a
4	ATF1	chr2:113470769-113471122	K562	blood:	n/a	n/a
5	BHLHE40	chr2:113470514-113471045	HepG2	liver:	n/a	n/a
6	BHLHE40	chr2:113470441-113471106	K562	blood:	n/a	n/a
7	CBX3	chr2:113476422-113476747	K562	blood:	n/a	n/a
8	CBX3	chr2:113478387-113478760	K562	blood:	n/a	n/a
9	CBX3	chr2:113470546-113471196	K562	blood:	n/a	n/a
10	CCNT2	chr2:113470531-113471058	K562	blood:	n/a	n/a
11	CEBPB	chr2:113470554-113470583	K562	blood:	n/a	n/a
12	CEBPB	chr2:113476641-113476668	IMR90	lung:	n/a	n/a
13	CEBPB	chr2:113470792-113471072	IMR90	lung:	n/a	n/a
14	CTCF	chr2:113476127-113476235	GM19238	blood:	n/a	n/a
15	CTCF	chr2:113476064-113476329	K562	blood:	n/a	n/a
16	CTCF	chr2:113476200-113476350	GM12871	blood:	n/a	n/a
17	CTCF	chr2:113470669-113470805	K562	blood:	n/a	n/a
18	CTCF	chr2:113476122-113476267	NHEK	skin:	n/a	n/a
19	CTCF	chr2:113471220-113471370	HCM	heart:	n/a	chr2:113471296-113471314 chr2:113471298-113471311
20	CTCF	chr2:113471280-113471430	HBMEC	blood vessel:	n/a	chr2:113471296-113471314 chr2:113471298-113471311
21	CTCF	chr2:113476069-113476356	K562	blood:	n/a	n/a
22	CTCF	chr2:113476171-113476235	GM20000	blood:	n/a	n/a
23	CTCF	chr2:113471200-113471350	HCPEpiC	choroid plexus:	n/a	chr2:113471296-113471314 chr2:113471298-113471311
24	CTCF	chr2:113476280-113476430	K562	blood:	n/a	n/a
25	CTCF	chr2:113476173-113476217	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr2:113470608-113470685	K562	blood:	n/a	n/a
27	CTCF	chr2:113476100-113476250	HepG2	liver:	n/a	n/a
28	CTCF	chr2:113476139-113476239	GM12878	blood:	n/a	n/a
29	CTCF	chr2:113476320-113476470	GM12873	blood:	n/a	n/a
30	CTCF	chr2:113476130-113476253	GM12892	blood:	n/a	n/a
31	CTCF	chr2:113476109-113476295	K562	blood:	n/a	n/a
32	CTCF	chr2:113476121-113476240	GM12878	blood:	n/a	n/a
33	CTCF	chr2:113476100-113476250	NHEK	skin:	n/a	n/a
34	CTCF	chr2:113470540-113470690	HepG2	liver:	n/a	n/a
35	CTCF	chr2:113476040-113476190	HMEC	breast:	n/a	n/a
36	CTCF	chr2:113476080-113476230	K562	blood:	n/a	n/a
37	CTCF	chr2:113476175-113476243	HepG2	liver:	n/a	n/a
38	CTCF	chr2:113476167-113476245	GM19239	blood:	n/a	n/a
39	CTCF	chr2:113476148-113476255	GM19240	blood:	n/a	n/a
40	CUX1	chr2:113470731-113471158	K562	blood:	n/a	n/a
41	E2F4	chr2:113477992-113478147	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr2:113472829-113473194	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F6	chr2:113478544-113478736	K562	blood:	n/a	n/a
44	EBF1	chr2:113469971-113470422	GM12878	blood:	n/a	chr2:113470236-113470245 chr2:113470234-113470247 chr2:113470235-113470246 chr2:113470236-113470245 chr2:113470236-113470246
45	EBF1	chr2:113470020-113470581	GM12878	blood:	n/a	chr2:113470236-113470245 chr2:113470234-113470247 chr2:113470235-113470246 chr2:113470236-113470245 chr2:113470236-113470246
46	EBF1	chr2:113470042-113470435	GM12878	blood:	n/a	chr2:113470236-113470245 chr2:113470234-113470247 chr2:113470235-113470246 chr2:113470236-113470245 chr2:113470236-113470246
47	EGR1	chr2:113470706-113471209	K562	blood:	n/a	n/a
48	EGR1	chr2:113470731-113471205	K562	blood:	n/a	n/a
49	ELF1	chr2:113470672-113471297	K562	blood:	n/a	n/a
50	EP300	chr2:113478513-113478621	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:113470704-113470754	HRPEpiC	eye:	n/a
2	chr2:113470704-113470754	HMEC	breast:	n/a
3	chr2:113470704-113470754	BE2_C	brain:	n/a
4	chr2:113470704-113470754	AG10803	skin:	n/a
5	chr2:113470704-113470754	LNCaP	prostate:	n/a
6	chr2:113470704-113470754	U87	brain:	n/a
7	chr2:113470704-113470754	PrEC	prostate:	n/a
8	chr2:113470704-113470754	NHDF-neo	bronchial:	n/a
9	chr2:113470704-113470754	MCF-7	breast:	n/a
10	chr2:113470704-113470754	BJ	skin:	n/a
11	chr2:113470704-113470754	HRCEpiC	kidney:	n/a
12	chr2:113470704-113470754	GM06990	blood:	n/a
13	chr2:113470704-113470754	HCM	heart:	n/a
14	chr2:113470704-113470754	HCF	heart:	n/a
15	chr2:113470704-113470754	Caco-2	colon:	n/a
16	chr2:113470704-113470754	SK-N-MC	brain:	n/a
17	chr2:113470704-113470754	RPTEC	kidney:	n/a
18	chr2:113470704-113470754	NHBE	bronchial:	n/a
19	chr2:113470704-113470754	AG09319	gingival:	n/a
20	chr2:113470704-113470754	GM12878	blood:	n/a
21	chr2:113470704-113470754	AoSMC	blood vessel:	n/a
22	chr2:113470704-113470754	SK-N-SH_RA	brain:	n/a
23	chr2:113470704-113470754	A549	lung:	n/a
24	chr2:113470704-113470754	HCT-116	colon:	n/a
25	chr2:113470704-113470754	PFSK-1	brain:	n/a
26	chr2:113470704-113470754	HNPCEpiC	eye:	n/a
27	chr2:113470704-113470754	PANC-1	pancreas:	n/a
28	chr2:113470704-113470754	NB4	blood:	n/a
29	chr2:113470704-113470754	HRE	kidney:	n/a
30	chr2:113470704-113470754	SK-N-SH	brain:	n/a
31	chr2:113470704-113470754	HEEpiC	esophagus:	n/a
32	chr2:113470704-113470754	SAEC	small airway:	n/a
33	chr2:113470704-113470754	CMK	blood:	n/a
34	chr2:113470704-113470754	Jurkat	blood:	n/a
35	chr2:113470704-113470754	T-47D	breast:	n/a
36	chr2:113470704-113470754	NT2-D1	testis:	n/a
37	chr2:113470704-113470754	AG04450	lung:	fetal
38	chr2:113470704-113470754	Hela-S3	cervix:	n/a
39	chr2:113470704-113470754	HL-60	blood:	n/a
40	chr2:113470704-113470754	ovcar-3	ovarian:	n/a
41	chr2:113470704-113470754	AG04449	skin:	fetal
42	chr2:113470704-113470754	NH-A	brain:	n/a
43	chr2:113470704-113470754	GM19239	blood:	n/a
44	chr2:113470704-113470754	ProgFib	skin:	n/a
45	chr2:113470704-113470754	IMR90	lung:	fetal
46	chr2:113470704-113470754	AG09309	skin:	n/a
47	chr2:113470704-113470754	HepG2	liver:	n/a
48	chr2:113470704-113470754	ECC-1	luminal epithelium:	n/a
49	chr2:113470704-113470754	GM12892	blood:	n/a
50	chr2:113470704-113470754	HIPEpiC	eye:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:113463436..113465065-chr2:113468008..113469803,2	K562	blood:
2	chr2:113414501..113417087-chr2:113468688..113471406,2	K562	blood:
3	chr2:113415587..113417242-chr2:113468748..113471406,3	K562	blood:
4	chr2:113357797..113359633-chr2:113475754..113478612,2	K562	blood:
5	chr2:113401638..113406636-chr2:113469377..113473888,9	K562	blood:
6	chr2:113477140..113479132-chr2:113479406..113481880,2	K562	blood:
7	chr2:113462767..113464610-chr2:113470290..113471852,2	K562	blood:
8	chr2:113468636..113470784-chr2:113471239..113473518,2	MCF-7	breast:
9	chr2:113465999..113468016-chr2:113469384..113470949,2	K562	blood:
10	chr2:113392494..113394338-chr2:113475169..113476676,2	MCF-7	breast:
11	chr2:113461776..113469381-chr2:113473397..113480932,10	K562	blood:
12	chr2:113463027..113465747-chr2:113466375..113467999,2	K562	blood:
13	chr2:113408522..113411073-chr2:113469156..113471009,2	K562	blood:
14	chr2:113468894..113470919-chr2:113476217..113478885,2	MCF-7	breast:
15	chr2:113423910..113425934-chr2:113475592..113478150,2	K562	blood:
16	chr2:113400575..113405879-chr2:113475243..113481233,15	K562	blood:
17	chr2:113443028..113446257-chr2:113466353..113468371,4	K562	blood:
18	chr2:113420962..113423174-chr2:113470482..113472440,2	K562	blood:
19	chr2:113470986..113471535-chr2:113484133..113484894,2	K562	blood:
20	chr2:113470817..113472423-chr2:113482357..113484049,2	K562	blood:
21	chr2:113458404..113460724-chr2:113468297..113470571,2	K562	blood:
22	chr2:113475474..113478098-chr2:113481097..113483249,3	MCF-7	breast:
23	chr2:113471766..113473686-chr2:113477982..113479580,2	MCF-7	breast:
24	chr2:113455109..113458679-chr2:113473651..113476820,4	K562	blood:
25	chr2:112896674..112899558-chr2:113471538..113473155,2	K562	blood:
26	chr2:113475206..113477952-chr4:173478464..173481229,2	K562	blood:
27	chr2:113456271..113458679-chr2:113474472..113476820,3	K562	blood:
28	chr2:113385104..113391547-chr2:113463938..113470179,6	K562	blood:
29	chr2:113462515..113465478-chr2:113468024..113470345,2	K562	blood:
30	chr2:113450086..113451690-chr2:113470849..113472489,2	K562	blood:
31	chr2:113468894..113470919-chr2:113476217..113478885,2	MCF-7	breast:
32	chr2:113470447..113473260-chr2:113504157..113506344,2	K562	blood:
33	chr2:113401171..113414378-chr2:113468812..113486672,46	K562	blood:
34	chr2:113470817..113472940-chr2:113481577..113484049,3	K562	blood:
35	chr2:113470616..113472582-chr2:113482683..113484318,2	MCF-7	breast:
36	chr2:113469794..113474486-chr2:113475351..113478319,4	K562	blood:
37	chr2:113469794..113474486-chr2:113475351..113478319,4	K562	blood:
38	chr2:113468636..113470784-chr2:113471239..113473518,2	MCF-7	breast:
39	chr2:113465999..113468016-chr2:113469384..113470949,2	K562	blood:

No data

Variant related genes	Relation type
NT5DC4	TF binding region
NT5DC4	CpG island
ENSG00000144136	chromatin interactions
ENSG00000144130	chromatin interactions
ENSG00000237753	chromatin interactions

Extended variants
information (count: 501 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:501 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561287740	chr2:113467784-113467785	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs11886267	chr2:113467799-113467800	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs60922517	chr2:113467819-113467820	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs7589102	chr2:113467827-113467828	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs187963464	chr2:113467862-113467863	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs145775100	chr2:113467868-113467869	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs192433125	chr2:113467918-113467919	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs199604888	chr2:113467919-113467920	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs6542084	chr2:113467920-113467921	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs556836464	chr2:113467955-113467956	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs192085876	chr2:113467986-113467987	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs184365299	chr2:113467992-113467993	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs140622233	chr2:113468006-113468007	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs145672735	chr2:113468041-113468042	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs572323822	chr2:113468061-113468062	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs6542085	chr2:113468076-113468077	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs189192002	chr2:113468104-113468105	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs529193696	chr2:113468105-113468106	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs386649251	chr2:113468112-113468113	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs138224452	chr2:113468114-113468115	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs531541505	chr2:113468143-113468144	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs551153334	chr2:113468153-113468154	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs182473228	chr2:113468171-113468172	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs62157382	chr2:113468189-113468190	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs547449770	chr2:113468213-113468214	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs567950732	chr2:113468214-113468215	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs187315745	chr2:113468264-113468265	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs77516749	chr2:113468293-113468294	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs6542087	chr2:113468328-113468329	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs576527617	chr2:113468329-113468330	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs189381521	chr2:113468346-113468347	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs143624812	chr2:113468362-113468363	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs148056423	chr2:113468371-113468372	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs141750296	chr2:113468396-113468397	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs150568565	chr2:113468467-113468468	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs75965985	chr2:113468508-113468509	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs542469597	chr2:113468557-113468558	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs80049391	chr2:113468644-113468645	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs531375092	chr2:113468654-113468655	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs181030228	chr2:113468699-113468700	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs564811516	chr2:113468716-113468717	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs538568106	chr2:113468725-113468726	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs115079172	chr2:113468744-113468745	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs558095475	chr2:113468875-113468876	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs58533146	chr2:113468896-113468897	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs373526133	chr2:113468971-113468972	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs564657708	chr2:113468989-113468990	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs550180028	chr2:113468998-113468999	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs570356700	chr2:113469000-113469001	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs72950325	chr2:113469024-113469025	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:66)

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	17483303	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
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	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
Acute lymphoblastic leukemia	18458336	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:147 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113458800-113469000	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr2:113462000-113468800	Enhancers	Primary hematopoietic stem cells	blood
3	chr2:113462600-113469400	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr2:113462800-113469200	Enhancers	Primary B cells from peripheral blood	blood
5	chr2:113463000-113469000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr2:113464200-113486400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr2:113465200-113470600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr2:113465400-113468800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr2:113465400-113469000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr2:113465400-113470400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr2:113465400-113470600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr2:113465400-113470600	Weak transcription	HMEC	breast
13	chr2:113465400-113470600	Weak transcription	NHEK	skin
14	chr2:113465600-113468600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr2:113465600-113470400	Enhancers	K562	blood
16	chr2:113465800-113470600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr2:113466600-113467800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr2:113466600-113467800	Enhancers	Spleen	Spleen
19	chr2:113466600-113468000	Bivalent Enhancer	Fetal Muscle Leg	muscle
20	chr2:113466600-113468000	Enhancers	GM12878-XiMat	blood
21	chr2:113466800-113468200	Enhancers	Primary B cells from cord blood	blood
22	chr2:113467200-113468200	Enhancers	Brain Anterior Caudate	brain
23	chr2:113467200-113468600	Enhancers	Brain Hippocampus Middle	brain
24	chr2:113467200-113468800	Enhancers	Brain Cingulate Gyrus	brain
25	chr2:113467200-113468800	Enhancers	Brain Substantia Nigra	brain
26	chr2:113467400-113467800	Enhancers	Brain Angular Gyrus	brain
27	chr2:113467400-113467800	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr2:113467400-113467800	Enhancers	Fetal Muscle Trunk	muscle
29	chr2:113467400-113467800	Enhancers	HSMMtube	muscle
30	chr2:113467400-113469200	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr2:113467600-113467800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr2:113467600-113468000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr2:113467600-113470600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr2:113467800-113470000	Weak transcription	Spleen	Spleen
35	chr2:113467800-113471000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr2:113468000-113470000	Weak transcription	GM12878-XiMat	blood
37	chr2:113468000-113470400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr2:113468200-113468600	Weak transcription	Brain Anterior Caudate	brain
39	chr2:113468600-113468800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr2:113468600-113468800	Enhancers	Brain Anterior Caudate	brain
41	chr2:113468800-113470600	Weak transcription	Primary hematopoietic stem cells	blood
42	chr2:113468800-113470600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr2:113468800-113470800	Weak transcription	Brain Anterior Caudate	brain
44	chr2:113468800-113472600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr2:113469000-113470400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr2:113469000-113470600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr2:113469000-113474600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr2:113469200-113469600	Weak transcription	Primary B cells from peripheral blood	blood
49	chr2:113469200-113470600	Weak transcription	Monocytes-CD14+_RO01746	blood
50	chr2:113469400-113471000	Weak transcription	Primary monocytes fromperipheralblood	blood

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