Variant report

Variant	esv3458162
Chromosome Location	chr2:113460460-113484652
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1324)
CpG islands
(count:245)
Chromatin interactive
region (count:102)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1324 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:113482567-113482699	K562	blood:	n/a	n/a
2	ARID3A	chr2:113470816-113471130	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:113484256-113484623	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:113482543-113482710	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:113463802-113464251	K562	blood:	n/a	n/a
6	ARID3A	chr2:113470854-113471064	K562	blood:	n/a	n/a
7	ARID3A	chr2:113484298-113484482	K562	blood:	n/a	n/a
8	ATF1	chr2:113476270-113476404	K562	blood:	n/a	n/a
9	ATF1	chr2:113470769-113471122	K562	blood:	n/a	n/a
10	ATF1	chr2:113463778-113464170	K562	blood:	n/a	n/a
11	ATF2	chr2:113464925-113466306	GM12878	blood:	n/a	n/a
12	ATF2	chr2:113484070-113484674	GM12878	blood:	n/a	n/a
13	ATF2	chr2:113465819-113466214	GM12878	blood:	n/a	n/a
14	ATF3	chr2:113463768-113464205	K562	blood:	n/a	n/a
15	BACH1	chr2:113484298-113484553	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr2:113463829-113464161	K562	blood:	n/a	n/a
17	BATF	chr2:113483428-113483798	GM12878	blood:	n/a	chr2:113483567-113483578 chr2:113483568-113483578
18	BATF	chr2:113463811-113464122	GM12878	blood:	n/a	n/a
19	BATF	chr2:113465673-113466208	GM12878	blood:	n/a	n/a
20	BATF	chr2:113483426-113483701	GM12878	blood:	n/a	chr2:113483567-113483578 chr2:113483568-113483578
21	BATF	chr2:113484287-113484572	GM12878	blood:	n/a	n/a
22	BATF	chr2:113465787-113466148	GM12878	blood:	n/a	n/a
23	BCL11A	chr2:113463860-113464116	GM12878	blood:	n/a	chr2:113464000-113464007
24	BCL11A	chr2:113465750-113466193	GM12878	blood:	n/a	n/a
25	BCL11A	chr2:113465826-113466133	GM12878	blood:	n/a	n/a
26	BCL3	chr2:113465813-113466182	GM12878	blood:	n/a	n/a
27	BCL3	chr2:113483384-113483839	GM12878	blood:	n/a	n/a
28	BCLAF1	chr2:113484194-113484679	GM12878	blood:	n/a	n/a
29	BCLAF1	chr2:113465627-113466276	GM12878	blood:	n/a	n/a
30	BCLAF1	chr2:113463707-113464241	GM12878	blood:	n/a	chr2:113464000-113464007
31	BCLAF1	chr2:113484212-113484684	GM12878	blood:	n/a	n/a
32	BCLAF1	chr2:113463694-113464236	K562	blood:	n/a	chr2:113464000-113464007
33	BHLHE40	chr2:113463529-113464298	K562	blood:	n/a	n/a
34	BHLHE40	chr2:113484261-113484644	HepG2	liver:	n/a	n/a
35	BHLHE40	chr2:113484273-113484609	K562	blood:	n/a	n/a
36	BHLHE40	chr2:113465642-113466217	GM12878	blood:	n/a	n/a
37	BHLHE40	chr2:113482327-113482732	K562	blood:	n/a	n/a
38	BHLHE40	chr2:113483533-113483755	K562	blood:	n/a	chr2:113483667-113483680
39	BHLHE40	chr2:113463323-113464170	GM12878	blood:	n/a	n/a
40	BHLHE40	chr2:113482264-113482788	HepG2	liver:	n/a	n/a
41	BHLHE40	chr2:113470441-113471106	K562	blood:	n/a	n/a
42	BHLHE40	chr2:113470514-113471045	HepG2	liver:	n/a	n/a
43	BHLHE40	chr2:113483385-113484660	GM12878	blood:	n/a	chr2:113483667-113483680
44	BHLHE40	chr2:113483018-113483049	K562	blood:	n/a	n/a
45	BHLHE40	chr2:113482477-113482564	GM12878	blood:	n/a	n/a
46	BHLHE40	chr2:113465087-113465306	K562	blood:	n/a	n/a
47	BHLHE40	chr2:113483441-113483918	HepG2	liver:	n/a	chr2:113483667-113483680
48	BRCA1	chr2:113484095-113484616	GM12878	blood:	n/a	n/a
49	BRCA1	chr2:113484245-113484642	HepG2	liver:	n/a	n/a
50	CBX3	chr2:113463384-113464303	K562	blood:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:113465072-113465122	T-47D	breast:	n/a
2	chr2:113465072-113465122	T-47D	breast:	n/a
3	chr2:113483728-113483778	NB4	blood:	n/a
4	chr2:113465072-113465122	HEEpiC	esophagus:	n/a
5	chr2:113464048-113464098	ProgFib	skin:	n/a
6	chr2:113464048-113464098	AoSMC	blood vessel:	n/a
7	chr2:113483728-113483778	SK-N-SH	brain:	n/a
8	chr2:113465072-113465122	HAEpiC	amniotic membrane:	n/a
9	chr2:113465072-113465122	GM19239	blood:	n/a
10	chr2:113465072-113465122	SAEC	small airway:	n/a
11	chr2:113464048-113464098	NB4	blood:	n/a
12	chr2:113470704-113470754	HIPEpiC	eye:	n/a
13	chr2:113483728-113483778	CMK	blood:	n/a
14	chr2:113470704-113470754	HepG2	liver:	n/a
15	chr2:113464048-113464098	Hela-S3	cervix:	n/a
16	chr2:113483728-113483778	GM12878	blood:	n/a
17	chr2:113465072-113465122	BE2_C	brain:	n/a
18	chr2:113465072-113465122	PANC-1	pancreas:	n/a
19	chr2:113470704-113470754	NHBE	bronchial:	n/a
20	chr2:113470704-113470754	GM12892	blood:	n/a
21	chr2:113465072-113465122	U87	brain:	n/a
22	chr2:113465072-113465122	Hela-S3	cervix:	n/a
23	chr2:113464048-113464098	Hepatocyte	liver:	n/a
24	chr2:113483728-113483778	HRPEpiC	eye:	n/a
25	chr2:113464048-113464098	RPTEC	kidney:	n/a
26	chr2:113483728-113483778	ECC-1	luminal epithelium:	n/a
27	chr2:113483728-113483778	PANC-1	pancreas:	n/a
28	chr2:113465072-113465122	SK-N-SH_RA	brain:	n/a
29	chr2:113470704-113470754	HL-60	blood:	n/a
30	chr2:113483728-113483778	U87	brain:	n/a
31	chr2:113470704-113470754	HMEC	breast:	n/a
32	chr2:113470704-113470754	HUVEC	blood vessel:	n/a
33	chr2:113465072-113465122	NB4	blood:	n/a
34	chr2:113465072-113465122	HIPEpiC	eye:	n/a
35	chr2:113483728-113483778	AG09319	gingival:	n/a
36	chr2:113483728-113483778	PrEC	prostate:	n/a
37	chr2:113465072-113465122	HCPEpiC	choroid plexus:	n/a
38	chr2:113464048-113464098	ovcar-3	ovarian:	n/a
39	chr2:113470704-113470754	SK-N-MC	brain:	n/a
40	chr2:113464048-113464098	NT2-D1	testis:	n/a
41	chr2:113464048-113464098	HCPEpiC	choroid plexus:	n/a
42	chr2:113465072-113465122	RPTEC	kidney:	n/a
43	chr2:113483728-113483778	AG04449	skin:	fetal
44	chr2:113465072-113465122	HRE	kidney:	n/a
45	chr2:113464048-113464098	AG09319	gingival:	n/a
46	chr2:113470704-113470754	K562	blood:	n/a
47	chr2:113465072-113465122	GM06990	blood:	n/a
48	chr2:113483728-113483778	NHBE	bronchial:	n/a
49	chr2:113470704-113470754	HAEpiC	amniotic membrane:	n/a
50	chr2:113464048-113464098	SK-N-SH_RA	brain:	n/a

(count:102 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:113460336..113462064-chr2:113462698..113465234,2	MCF-7	breast:
2	chr2:113462515..113465478-chr2:113468024..113470345,2	K562	blood:
3	chr2:113462515..113465478-chr2:113468024..113470345,2	K562	blood:
4	chr2:113446769..113452405-chr2:113453017..113461667,12	K562	blood:
5	chr2:113475474..113478098-chr2:113481097..113483249,3	MCF-7	breast:
6	chr2:113477140..113479132-chr2:113479406..113481880,2	K562	blood:
7	chr2:113455109..113458679-chr2:113473651..113476820,4	K562	blood:
8	chr2:113340042..113340549-chr2:113483924..113484572,2	K562	blood:
9	chr2:113471766..113473686-chr2:113477982..113479580,2	MCF-7	breast:
10	chr2:113484028..113484731-chr2:113642145..113642705,2	K562	blood:
11	chr2:113465999..113468016-chr2:113469384..113470949,2	K562	blood:
12	chr2:113401171..113414378-chr2:113468812..113486672,46	K562	blood:
13	chr2:113468636..113470784-chr2:113471239..113473518,2	MCF-7	breast:
14	chr2:113385104..113391547-chr2:113463938..113470179,6	K562	blood:
15	chr2:113357421..113358433-chr2:113481851..113482761,4	K562	blood:
16	chr2:113440346..113442226-chr2:113462249..113464616,2	K562	blood:
17	chr2:113477140..113479132-chr2:113479406..113481880,2	K562	blood:
18	chr2:113401638..113406636-chr2:113469377..113473888,9	K562	blood:
19	chr2:113480533..113482697-chr2:113482909..113484492,2	K562	blood:
20	chr2:113450165..113451078-chr2:113482472..113483036,2	MCF-7	breast:
21	chr2:113456271..113458679-chr2:113474472..113476820,3	K562	blood:
22	chr2:113421228..113422950-chr2:113462402..113464448,2	K562	blood:
23	chr2:113443028..113446257-chr2:113466353..113468371,4	K562	blood:
24	chr2:113384015..113385213-chr2:113482175..113483476,11	MCF-7	breast:
25	chr2:113414501..113417087-chr2:113468688..113471406,2	K562	blood:
26	chr2:113478980..113481125-chr2:113482565..113484434,2	MCF-7	breast:
27	chr2:113401472..113405460-chr2:113462823..113466044,10	K562	blood:
28	chr2:113340714..113343330-chr2:113462470..113465365,2	K562	blood:
29	chr2:113462523..113464029-chr2:113482070..113484503,2	MCF-7	breast:
30	chr2:113448136..113451389-chr2:113461614..113465494,4	K562	blood:
31	chr2:113338959..113342918-chr2:113483353..113487579,5	K562	blood:
32	chr2:113339955..113341936-chr2:113481777..113484601,3	MCF-7	breast:
33	chr2:113382749..113384471-chr2:113464194..113466806,2	K562	blood:
34	chr2:113462767..113464610-chr2:113470290..113471852,2	K562	blood:
35	chr2:113470986..113471535-chr2:113484133..113484894,2	K562	blood:
36	chr2:113463027..113465747-chr2:113466375..113467999,2	K562	blood:
37	chr2:113469794..113474486-chr2:113475351..113478319,4	K562	blood:
38	chr2:113423910..113425934-chr2:113475592..113478150,2	K562	blood:
39	chr2:113470986..113471535-chr2:113484133..113484894,2	K562	blood:
40	chr2:113403381..113406309-chr2:113461047..113462788,2	K562	blood:
41	chr2:113461776..113469381-chr2:113473397..113480932,10	K562	blood:
42	chr2:113458404..113460724-chr2:113468297..113470571,2	K562	blood:
43	chr2:113450086..113451690-chr2:113470849..113472489,2	K562	blood:
44	chr2:113420962..113423174-chr2:113470482..113472440,2	K562	blood:
45	chr2:113380065..113382456-chr2:113480700..113483703,3	MCF-7	breast:
46	chr2:113463436..113465065-chr2:113468008..113469803,2	K562	blood:
47	chr2:112655628..112656155-chr2:113481753..113482328,2	K562	blood:
48	chr2:113482871..113484637-chr2:113485555..113488424,2	K562	blood:
49	chr2:113468894..113470919-chr2:113476217..113478885,2	MCF-7	breast:
50	chr2:113468894..113470919-chr2:113476217..113478885,2	MCF-7	breast:

No data

Variant related genes	Relation type
NT5DC4	TF binding region
NT5DC4	CpG island
ENSG00000125630	chromatin interactions
ENSG00000144136	chromatin interactions
ENSG00000153208	chromatin interactions
ENSG00000144130	chromatin interactions
ENSG00000125611	chromatin interactions
ENSG00000237753	chromatin interactions
ENSG00000114999	chromatin interactions

Extended variants
information (count: 1093 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1093 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138455827	chr2:113460461-113460462	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs111664047	chr2:113460485-113460486	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs79536031	chr2:113460545-113460546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141901430	chr2:113460564-113460565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540873947	chr2:113460595-113460596	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373748090	chr2:113460610-113460611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560631166	chr2:113460614-113460615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs529454419	chr2:113460624-113460625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549621113	chr2:113460650-113460651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs150631151	chr2:113460659-113460660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs78451725	chr2:113460670-113460671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs551788076	chr2:113460704-113460705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs138722202	chr2:113460732-113460733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs76634961	chr2:113460798-113460799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs398080508	chr2:113460799-113460800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs139307752	chr2:113460816-113460817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs113331074	chr2:113460819-113460820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs546840310	chr2:113460872-113460873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs566675498	chr2:113460939-113460940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs183677131	chr2:113461007-113461008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555179938	chr2:113461016-113461017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs111453398	chr2:113461021-113461022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574987838	chr2:113461025-113461026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149348851	chr2:113461076-113461077	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs114947353	chr2:113461080-113461081	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs577523098	chr2:113461081-113461082	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs188193332	chr2:113461115-113461116	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs543756464	chr2:113461137-113461138	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs180986417	chr2:113461171-113461172	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs574279300	chr2:113461183-113461184	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs543226864	chr2:113461207-113461208	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs115596021	chr2:113461223-113461224	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs186309243	chr2:113461230-113461231	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs545478863	chr2:113461236-113461237	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs190041687	chr2:113461249-113461250	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs527657198	chr2:113461261-113461262	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs4848291	chr2:113461264-113461265	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs566746107	chr2:113461265-113461266	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs146041748	chr2:113461301-113461302	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs548766236	chr2:113461305-113461306	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs181491346	chr2:113461315-113461316	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs187015205	chr2:113461321-113461322	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs139962461	chr2:113461324-113461325	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs571273993	chr2:113461356-113461357	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs370001962	chr2:113461364-113461365	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs143407263	chr2:113461372-113461373	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs536960436	chr2:113461385-113461386	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs375545087	chr2:113461419-113461420	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs528199920	chr2:113461439-113461440	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs190767086	chr2:113461469-113461470	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:436 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113451800-113462800	Weak transcription	Dnd41	blood
2	chr2:113454800-113460600	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr2:113458600-113463400	Weak transcription	Osteobl	bone
4	chr2:113458600-113464000	Weak transcription	Brain Hippocampus Middle	brain
5	chr2:113458800-113460600	Weak transcription	Fetal Brain Female	brain
6	chr2:113458800-113463400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr2:113458800-113469000	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr2:113459400-113463400	Weak transcription	Primary B cells from cord blood	blood
9	chr2:113459600-113463000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr2:113459600-113463200	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr2:113459800-113463600	Weak transcription	NHLF	lung
12	chr2:113460000-113460800	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr2:113460000-113462000	Weak transcription	Primary hematopoietic stem cells	blood
14	chr2:113460000-113462400	Weak transcription	K562	blood
15	chr2:113460000-113463000	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr2:113460200-113462000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr2:113460200-113462600	Weak transcription	GM12878-XiMat	blood
18	chr2:113460200-113462800	Weak transcription	Primary B cells from peripheral blood	blood
19	chr2:113460600-113460800	Enhancers	Fetal Brain Female	brain
20	chr2:113460600-113462600	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr2:113460800-113462800	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr2:113462000-113464200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr2:113462000-113468800	Enhancers	Primary hematopoietic stem cells	blood
24	chr2:113462400-113462800	Enhancers	K562	blood
25	chr2:113462400-113465600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr2:113462600-113463400	Enhancers	GM12878-XiMat	blood
27	chr2:113462600-113469400	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr2:113462800-113463000	Flanking Active TSS	K562	blood
29	chr2:113462800-113463400	Enhancers	Dnd41	blood
30	chr2:113462800-113463400	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr2:113462800-113464400	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr2:113462800-113465400	Enhancers	HMEC	breast
33	chr2:113462800-113469200	Enhancers	Primary B cells from peripheral blood	blood
34	chr2:113463000-113463400	Enhancers	K562	blood
35	chr2:113463000-113464200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr2:113463000-113464400	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr2:113463000-113465800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr2:113463000-113469000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr2:113463200-113463400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
40	chr2:113463200-113463400	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr2:113463200-113463600	Bivalent Enhancer	NH-A	brain
42	chr2:113463200-113464200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
43	chr2:113463200-113464200	Enhancers	Thymus	Thymus
44	chr2:113463200-113464400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr2:113463200-113464400	Enhancers	Spleen	Spleen
46	chr2:113463200-113464600	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr2:113463200-113465000	Enhancers	Fetal Thymus	thymus
48	chr2:113463200-113465200	Enhancers	Primary neutrophils fromperipheralblood	blood
49	chr2:113463200-113465400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr2:113463200-113465400	Enhancers	NHEK	skin

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