Variant report

Variant	esv2759084
Chromosome Location	chr2:113469235-113478889
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:166)
CpG islands
(count:61)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:166 , 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	chr2:113470816-113471130	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:113470854-113471064	K562	blood:	n/a	n/a
3	ATF1	chr2:113470769-113471122	K562	blood:	n/a	n/a
4	ATF1	chr2:113476270-113476404	K562	blood:	n/a	n/a
5	BHLHE40	chr2:113470441-113471106	K562	blood:	n/a	n/a
6	BHLHE40	chr2:113470514-113471045	HepG2	liver:	n/a	n/a
7	CBX3	chr2:113478387-113478760	K562	blood:	n/a	n/a
8	CBX3	chr2:113470546-113471196	K562	blood:	n/a	n/a
9	CBX3	chr2:113476422-113476747	K562	blood:	n/a	n/a
10	CCNT2	chr2:113470531-113471058	K562	blood:	n/a	n/a
11	CEBPB	chr2:113470792-113471072	IMR90	lung:	n/a	n/a
12	CEBPB	chr2:113476641-113476668	IMR90	lung:	n/a	n/a
13	CEBPB	chr2:113470554-113470583	K562	blood:	n/a	n/a
14	CTCF	chr2:113476121-113476240	GM12878	blood:	n/a	n/a
15	CTCF	chr2:113470540-113470690	HepG2	liver:	n/a	n/a
16	CTCF	chr2:113476139-113476239	GM12878	blood:	n/a	n/a
17	CTCF	chr2:113476069-113476356	K562	blood:	n/a	n/a
18	CTCF	chr2:113471200-113471350	HCPEpiC	choroid plexus:	n/a	chr2:113471296-113471314 chr2:113471298-113471311
19	CTCF	chr2:113476320-113476470	GM12873	blood:	n/a	n/a
20	CTCF	chr2:113471280-113471430	HBMEC	blood vessel:	n/a	chr2:113471296-113471314 chr2:113471298-113471311
21	CTCF	chr2:113476100-113476250	NHEK	skin:	n/a	n/a
22	CTCF	chr2:113471220-113471370	HCM	heart:	n/a	chr2:113471296-113471314 chr2:113471298-113471311
23	CTCF	chr2:113476064-113476329	K562	blood:	n/a	n/a
24	CTCF	chr2:113476173-113476217	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr2:113476200-113476350	GM12871	blood:	n/a	n/a
26	CTCF	chr2:113470608-113470685	K562	blood:	n/a	n/a
27	CTCF	chr2:113476171-113476235	GM20000	blood:	n/a	n/a
28	CTCF	chr2:113476100-113476250	HepG2	liver:	n/a	n/a
29	CTCF	chr2:113476167-113476245	GM19239	blood:	n/a	n/a
30	CTCF	chr2:113476080-113476230	K562	blood:	n/a	n/a
31	CTCF	chr2:113476040-113476190	HMEC	breast:	n/a	n/a
32	CTCF	chr2:113476280-113476430	K562	blood:	n/a	n/a
33	CTCF	chr2:113476127-113476235	GM19238	blood:	n/a	n/a
34	CTCF	chr2:113470669-113470805	K562	blood:	n/a	n/a
35	CTCF	chr2:113476148-113476255	GM19240	blood:	n/a	n/a
36	CTCF	chr2:113476122-113476267	NHEK	skin:	n/a	n/a
37	CTCF	chr2:113476175-113476243	HepG2	liver:	n/a	n/a
38	CTCF	chr2:113476109-113476295	K562	blood:	n/a	n/a
39	CTCF	chr2:113476130-113476253	GM12892	blood:	n/a	n/a
40	CUX1	chr2:113470731-113471158	K562	blood:	n/a	n/a
41	E2F4	chr2:113472829-113473194	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr2:113477992-113478147	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F6	chr2:113478544-113478736	K562	blood:	n/a	n/a
44	E2F6	chr2:113478789-113479039	K562	blood:	n/a	n/a
45	EBF1	chr2:113470042-113470435	GM12878	blood:	n/a	chr2:113470236-113470245 chr2:113470234-113470247 chr2:113470235-113470246 chr2:113470236-113470245 chr2:113470236-113470246
46	EBF1	chr2:113470020-113470581	GM12878	blood:	n/a	chr2:113470236-113470245 chr2:113470234-113470247 chr2:113470235-113470246 chr2:113470236-113470245 chr2:113470236-113470246
47	EBF1	chr2:113469971-113470422	GM12878	blood:	n/a	chr2:113470236-113470245 chr2:113470234-113470247 chr2:113470235-113470246 chr2:113470236-113470245 chr2:113470236-113470246
48	EGR1	chr2:113470731-113471205	K562	blood:	n/a	n/a
49	EGR1	chr2:113470706-113471209	K562	blood:	n/a	n/a
50	ELF1	chr2:113470672-113471297	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	NB4	blood:	n/a
2	chr2:113470704-113470754	SK-N-SH_RA	brain:	n/a
3	chr2:113470704-113470754	MCF10A-Er-Src	breast:	n/a
4	chr2:113470704-113470754	NHDF-neo	bronchial:	n/a
5	chr2:113470704-113470754	T-47D	breast:	n/a
6	chr2:113470704-113470754	HRE	kidney:	n/a
7	chr2:113470704-113470754	MCF-7	breast:	n/a
8	chr2:113470704-113470754	AG04449	skin:	fetal
9	chr2:113470704-113470754	CMK	blood:	n/a
10	chr2:113470704-113470754	H1-hESC	embryonic stem cell:	embryo
11	chr2:113470704-113470754	SK-N-SH	brain:	n/a
12	chr2:113470704-113470754	GM12878	blood:	n/a
13	chr2:113470704-113470754	HMEC	breast:	n/a
14	chr2:113470704-113470754	HepG2	liver:	n/a
15	chr2:113470704-113470754	AG10803	skin:	n/a
16	chr2:113470704-113470754	U87	brain:	n/a
17	chr2:113470704-113470754	LNCaP	prostate:	n/a
18	chr2:113470704-113470754	GM06990	blood:	n/a
19	chr2:113470704-113470754	HCT-116	colon:	n/a
20	chr2:113470704-113470754	K562	blood:	n/a
21	chr2:113470704-113470754	HIPEpiC	eye:	n/a
22	chr2:113470704-113470754	HCM	heart:	n/a
23	chr2:113470704-113470754	Jurkat	blood:	n/a
24	chr2:113470704-113470754	PFSK-1	brain:	n/a
25	chr2:113470704-113470754	HRCEpiC	kidney:	n/a
26	chr2:113470704-113470754	GM12892	blood:	n/a
27	chr2:113470704-113470754	HCPEpiC	choroid plexus:	n/a
28	chr2:113470704-113470754	HPAEpiC	pulmonary alveolar:	n/a
29	chr2:113470704-113470754	AoSMC	blood vessel:	n/a
30	chr2:113470704-113470754	AG04450	lung:	fetal
31	chr2:113470704-113470754	IMR90	lung:	fetal
32	chr2:113470704-113470754	HEK293	kidney:	embryo
33	chr2:113470704-113470754	HCF	heart:	n/a
34	chr2:113470704-113470754	Caco-2	colon:	n/a
35	chr2:113470704-113470754	SAEC	small airway:	n/a
36	chr2:113470704-113470754	SKMC	muscle:	n/a
37	chr2:113470704-113470754	Hepatocyte	liver:	n/a
38	chr2:113470704-113470754	GM19239	blood:	n/a
39	chr2:113470704-113470754	A549	lung:	n/a
40	chr2:113470704-113470754	BE2_C	brain:	n/a
41	chr2:113470704-113470754	RPTEC	kidney:	n/a
42	chr2:113470704-113470754	HNPCEpiC	eye:	n/a
43	chr2:113470704-113470754	BJ	skin:	n/a
44	chr2:113470704-113470754	ECC-1	luminal epithelium:	n/a
45	chr2:113470704-113470754	NH-A	brain:	n/a
46	chr2:113470704-113470754	HAEpiC	amniotic membrane:	n/a
47	chr2:113470704-113470754	PrEC	prostate:	n/a
48	chr2:113470704-113470754	Hela-S3	cervix:	n/a
49	chr2:113470704-113470754	SK-N-MC	brain:	n/a
50	chr2:113470704-113470754	NHBE	bronchial:	n/a

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

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

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: 448 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:448 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2176321	chr2:113469235-113469236	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs541094043	chr2:113469280-113469281	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs560989363	chr2:113469282-113469283	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs529692947	chr2:113469347-113469348	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs549785185	chr2:113469353-113469354	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs190265857	chr2:113469426-113469427	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs56350405	chr2:113469439-113469440	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs540806072	chr2:113469442-113469443	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs4353893	chr2:113469482-113469483	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs55884358	chr2:113469515-113469516	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs539672209	chr2:113469542-113469543	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs182893060	chr2:113469605-113469606	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs375087014	chr2:113469614-113469615	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs2901943	chr2:113469616-113469617	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs2176320	chr2:113469629-113469630	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs537033866	chr2:113469666-113469667	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs144298144	chr2:113469670-113469671	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs576254457	chr2:113469677-113469678	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs538879152	chr2:113469688-113469689	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs558906452	chr2:113469783-113469784	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs2861386	chr2:113469799-113469800	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs541255967	chr2:113469801-113469802	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs370116704	chr2:113469811-113469812	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs560950757	chr2:113469822-113469823	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs574627962	chr2:113469824-113469825	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs146574494	chr2:113469830-113469831	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs141253580	chr2:113469841-113469842	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs563250464	chr2:113469887-113469888	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs532023884	chr2:113469911-113469912	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs552798371	chr2:113469940-113469941	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs150187781	chr2:113469941-113469942	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs559638708	chr2:113469944-113469945	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs74817873	chr2:113469979-113469980	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs74856234	chr2:113469989-113469990	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs539535629	chr2:113470004-113470005	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs138695742	chr2:113470007-113470008	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs537598077	chr2:113470011-113470012	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs149116498	chr2:113470024-113470025	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs570791460	chr2:113470037-113470038	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs539472265	chr2:113470038-113470039	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs143164495	chr2:113470048-113470049	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs556294794	chr2:113470081-113470082	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs116012996	chr2:113470088-113470089	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs534803286	chr2:113470117-113470118	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs554853843	chr2:113470127-113470128	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs6720627	chr2:113470146-113470147	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs908547	chr2:113470159-113470160	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs186167784	chr2:113470175-113470176	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs191878901	chr2:113470197-113470198	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs545421765	chr2:113470200-113470201	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	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:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113462600-113469400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr2:113464200-113486400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr2:113465200-113470600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr2:113465400-113470400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr2:113465400-113470600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr2:113465400-113470600	Weak transcription	HMEC	breast
7	chr2:113465400-113470600	Weak transcription	NHEK	skin
8	chr2:113465600-113470400	Enhancers	K562	blood
9	chr2:113465800-113470600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr2:113467600-113470600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr2:113467800-113470000	Weak transcription	Spleen	Spleen
12	chr2:113467800-113471000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr2:113468000-113470000	Weak transcription	GM12878-XiMat	blood
14	chr2:113468000-113470400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr2:113468800-113470600	Weak transcription	Primary hematopoietic stem cells	blood
16	chr2:113468800-113470600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr2:113468800-113470800	Weak transcription	Brain Anterior Caudate	brain
18	chr2:113468800-113472600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr2:113469000-113470400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr2:113469000-113470600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr2:113469000-113474600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr2:113469200-113469600	Weak transcription	Primary B cells from peripheral blood	blood
23	chr2:113469200-113470600	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr2:113469400-113471000	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr2:113469400-113484200	Weak transcription	Right Atrium	heart
26	chr2:113469600-113471400	Enhancers	Primary B cells from peripheral blood	blood
27	chr2:113469800-113471000	Enhancers	Fetal Kidney	kidney
28	chr2:113469800-113471600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr2:113470000-113470600	Enhancers	GM12878-XiMat	blood
30	chr2:113470000-113471400	Enhancers	NHDF-Ad	bronchial
31	chr2:113470000-113471800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr2:113470000-113471800	Enhancers	Spleen	Spleen
33	chr2:113470200-113471000	Bivalent Enhancer	HepG2	liver
34	chr2:113470200-113471400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr2:113470200-113471400	Enhancers	NHLF	lung
36	chr2:113470200-113471600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr2:113470400-113471000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
38	chr2:113470400-113471200	Flanking Active TSS	K562	blood
39	chr2:113470400-113471400	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr2:113470400-113471600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr2:113470400-113471600	Enhancers	NH-A	brain
42	chr2:113470400-113471600	Enhancers	Osteobl	bone
43	chr2:113470400-113471800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr2:113470600-113470800	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
45	chr2:113470600-113470800	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr2:113470600-113471000	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr2:113470600-113471200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr2:113470600-113471200	Enhancers	Primary hematopoietic stem cells	blood
49	chr2:113470600-113471200	Enhancers	HMEC	breast
50	chr2:113470600-113471400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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