Variant report

Variant	nsv1003372
Chromosome Location	chr2:113670890-113682621
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	ATF1	chr2:113678475-113678792	K562	blood:	n/a	n/a
2	BACH1	chr2:113681268-113681532	K562	blood:	n/a	n/a
3	BATF	chr2:113674183-113674484	GM12878	blood:	n/a	n/a
4	BHLHE40	chr2:113682108-113682201	K562	blood:	n/a	n/a
5	CBX3	chr2:113678342-113678908	HCT-116	colon:	n/a	n/a
6	CCNT2	chr2:113677966-113677977	K562	blood:	n/a	n/a
7	CEBPB	chr2:113681553-113681794	H1-hESC	embryonic stem cell:	n/a	chr2:113681704-113681715
8	CEBPB	chr2:113681548-113681860	HepG2	liver:	n/a	chr2:113681704-113681715
9	CEBPB	chr2:113681575-113681836	IMR90	lung:	n/a	chr2:113681704-113681715
10	CEBPB	chr2:113681359-113681873	K562	blood:	n/a	chr2:113681704-113681715
11	CEBPB	chr2:113681513-113681893	K562	blood:	n/a	chr2:113681704-113681715
12	CEBPB	chr2:113681552-113681752	A549	lung:	n/a	chr2:113681704-113681715
13	CREB1	chr2:113678400-113678795	K562	blood:	n/a	n/a
14	CTCF	chr2:113678760-113678910	HCFaa	heart:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
15	CTCF	chr2:113678700-113678850	AG10803	skin:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
16	CTCF	chr2:113681000-113681150	HMEC	breast:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
17	CTCF	chr2:113680980-113681130	NHEK	skin:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
18	CTCF	chr2:113680960-113681110	HBMEC	blood vessel:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
19	CTCF	chr2:113678730-113678743	K562	blood:	n/a	n/a
20	CTCF	chr2:113673580-113673730	GM12875	blood:	n/a	n/a
21	CTCF	chr2:113678700-113678850	HCM	heart:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
22	CTCF	chr2:113678760-113678910	HPAF	blood vessel:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
23	CTCF	chr2:113680960-113681110	HPAF	blood vessel:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
24	CTCF	chr2:113678720-113678870	HMF	breast:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
25	CTCF	chr2:113678760-113678910	HCPEpiC	choroid plexus:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
26	CTCF	chr2:113678760-113678910	HFF	foreskin:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
27	CTCF	chr2:113682140-113682290	GM12867	blood:	n/a	n/a
28	CTCF	chr2:113680994-113681105	K562	blood:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
29	CTCF	chr2:113678761-113678832	NHEK	skin:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
30	CTCF	chr2:113681060-113681210	HMF	breast:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
31	CTCF	chr2:113680980-113681130	HPAF	blood vessel:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
32	CTCF	chr2:113678700-113678850	HCPEpiC	choroid plexus:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
33	CTCF	chr2:113678760-113678910	HBMEC	blood vessel:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
34	CTCF	chr2:113681042-113681197	K562	blood:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
35	CTCF	chr2:113681060-113681210	HCPEpiC	choroid plexus:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
36	CTCF	chr2:113680980-113681130	AoAF	blood vessel:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
37	CTCF	chr2:113681040-113681190	HAc	cerebellar:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
38	CTCF	chr2:113678760-113678910	HCT-116	colon:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
39	CTCF	chr2:113678720-113678870	HPAF	blood vessel:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
40	CTCF	chr2:113678660-113678810	NHEK	skin:	n/a	n/a
41	CTCF	chr2:113681054-113681101	NHEK	skin:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
42	CTCF	chr2:113678700-113678850	HBMEC	blood vessel:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
43	CTCF	chr2:113681000-113681150	HEEpiC	esophagus:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
44	CTCF	chr2:113680980-113681130	HCFaa	heart:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
45	EP300	chr2:113681175-113681530	K562	blood:	n/a	n/a
46	ESR1	chr2:113676732-113677025	ECC-1	luminal epithelium:	n/a	chr2:113676856-113676871
47	FOS	chr2:113678481-113678768	MCF10A-Er-Src	breast:	n/a	chr2:113678613-113678623 chr2:113678613-113678623 chr2:113678636-113678643 chr2:113678613-113678623
48	FOS	chr2:113678462-113678784	MCF10A-Er-Src	breast:	n/a	chr2:113678613-113678623 chr2:113678613-113678623 chr2:113678636-113678643 chr2:113678613-113678623
49	FOS	chr2:113678469-113678819	MCF10A-Er-Src	breast:	n/a	chr2:113678613-113678623 chr2:113678613-113678623 chr2:113678636-113678643 chr2:113678613-113678623
50	FOS	chr2:113678470-113678810	MCF10A-Er-Src	breast:	n/a	chr2:113678613-113678623 chr2:113678613-113678623 chr2:113678636-113678643 chr2:113678613-113678623

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:113676413-113676463	MCF10A-Er-Src	breast:	n/a
2	chr2:113671813-113671863	U87	brain:	n/a
3	chr2:113676235-113676285	LNCaP	prostate:	n/a
4	chr2:113671813-113671863	AG10803	skin:	n/a
5	chr2:113671356-113671406	ovcar-3	ovarian:	n/a
6	chr2:113676413-113676463	ovcar-3	ovarian:	n/a
7	chr2:113672758-113672808	AG09309	skin:	n/a
8	chr2:113676235-113676285	A549	lung:	n/a
9	chr2:113672199-113672249	ovcar-3	ovarian:	n/a
10	chr2:113671356-113671406	HL-60	blood:	n/a
11	chr2:113672758-113672808	GM12892	blood:	n/a
12	chr2:113672587-113672637	IMR90	lung:	fetal
13	chr2:113671356-113671406	SK-N-SH	brain:	n/a
14	chr2:113672713-113672763	GM12891	blood:	n/a
15	chr2:113672199-113672249	SAEC	small airway:	n/a
16	chr2:113676235-113676285	U87	brain:	n/a
17	chr2:113676235-113676285	SK-N-SH_RA	brain:	n/a
18	chr2:113672587-113672637	HAEpiC	amniotic membrane:	n/a
19	chr2:113676413-113676463	Jurkat	blood:	n/a
20	chr2:113672587-113672637	Caco-2	colon:	n/a
21	chr2:113671813-113671863	NT2-D1	testis:	n/a
22	chr2:113671356-113671406	AoSMC	blood vessel:	n/a
23	chr2:113676413-113676463	GM12878	blood:	n/a
24	chr2:113676413-113676463	HMEC	breast:	n/a
25	chr2:113672713-113672763	SAEC	small airway:	n/a
26	chr2:113671813-113671863	HIPEpiC	eye:	n/a
27	chr2:113676413-113676463	Hela-S3	cervix:	n/a
28	chr2:113672199-113672249	GM06990	blood:	n/a
29	chr2:113672758-113672808	MCF10A-Er-Src	breast:	n/a
30	chr2:113671813-113671863	SK-N-MC	brain:	n/a
31	chr2:113672758-113672808	ProgFib	skin:	n/a
32	chr2:113671356-113671406	HPAEpiC	pulmonary alveolar:	n/a
33	chr2:113676413-113676463	Caco-2	colon:	n/a
34	chr2:113672758-113672808	HAEpiC	amniotic membrane:	n/a
35	chr2:113672587-113672637	NHBE	bronchial:	n/a
36	chr2:113672713-113672763	RPTEC	kidney:	n/a
37	chr2:113672758-113672808	HEK293	kidney:	embryo
38	chr2:113671813-113671863	HEEpiC	esophagus:	n/a
39	chr2:113672199-113672249	SK-N-MC	brain:	n/a
40	chr2:113672758-113672808	HCT-116	colon:	n/a
41	chr2:113676235-113676285	NHDF-neo	bronchial:	n/a
42	chr2:113671356-113671406	ECC-1	luminal epithelium:	n/a
43	chr2:113672199-113672249	PANC-1	pancreas:	n/a
44	chr2:113676413-113676463	HCPEpiC	choroid plexus:	n/a
45	chr2:113671356-113671406	HMEC	breast:	n/a
46	chr2:113672199-113672249	HMEC	breast:	n/a
47	chr2:113672587-113672637	HepG2	liver:	n/a
48	chr2:113676235-113676285	AG09309	skin:	n/a
49	chr2:113672758-113672808	SK-N-MC	brain:	n/a
50	chr2:113676235-113676285	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr2:113674868..113678484-chr2:113678490..113681949,3	K562	blood:
2	chr2:113671840..113673562-chr2:113673585..113676227,2	K562	blood:
3	chr2:113682507..113685123-chr2:113688848..113691185,2	K562	blood:
4	chr2:113488382..113489971-chr2:113681773..113683855,2	MCF-7	breast:
5	chr2:113674868..113678484-chr2:113678490..113681949,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL37-2	chr2:113679974-113683444	ucscGeneNc_uc002tji_1

Variant related genes	Relation type
IL37	TF binding region
IL37	CpG island
ENSG00000125571	chromatin interactions
ENSG00000227368	chromatin interactions

Extended variants
information (count: 537 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:537 , 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	rs2723168	chr2:113670890-113670891	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568352582	chr2:113670924-113670925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536191651	chr2:113670940-113670941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs2708957	chr2:113670949-113670950	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs559271754	chr2:113670962-113670963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575839511	chr2:113670967-113670968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183019836	chr2:113670969-113670970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2708956	chr2:113670978-113670979	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs572141847	chr2:113670991-113670992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs540762065	chr2:113670999-113671000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs2708955	chr2:113671002-113671003	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs574440520	chr2:113671003-113671004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs386649264	chr2:113671012-113671013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs386649265	chr2:113671013-113671014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs2466449	chr2:113671014-113671015	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs559361504	chr2:113671019-113671020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552765437	chr2:113671025-113671026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs6739660	chr2:113671026-113671027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192984916	chr2:113671082-113671083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2464913	chr2:113671136-113671137	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs528625021	chr2:113671146-113671147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551548690	chr2:113671177-113671178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548388395	chr2:113671184-113671185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs568116243	chr2:113671185-113671186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2466448	chr2:113671198-113671199	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs549677450	chr2:113671288-113671289	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs148098012	chr2:113671297-113671298	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs3811045	chr2:113671303-113671304	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs373718600	chr2:113671331-113671332	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs28947189	chr2:113671332-113671333	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs528949769	chr2:113671344-113671345	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs377121293	chr2:113671356-113671357	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs140928473	chr2:113671372-113671373	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs375091029	chr2:113671373-113671374	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs3811046	chr2:113671378-113671379	Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs375280608	chr2:113671383-113671384	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs184647177	chr2:113671389-113671390	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
38	rs372712283	chr2:113671393-113671394	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs3811047	chr2:113671410-113671411	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs149966581	chr2:113671413-113671414	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs375647231	chr2:113671441-113671442	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs200782323	chr2:113671442-113671443	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs376337700	chr2:113671472-113671473	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs138501808	chr2:113671484-113671485	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs3811048	chr2:113671518-113671519	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs79683662	chr2:113671549-113671550	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs371943356	chr2:113671554-113671555	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs189445938	chr2:113671594-113671595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528629358	chr2:113671621-113671622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs192603581	chr2:113671638-113671639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Cancer	17699850	CNVD
Ovarian cancer	17699850	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113664800-113678000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr2:113671400-113671600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:113671600-113674400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr2:113671600-113674800	Enhancers	Primary T cells fromperipheralblood	blood
5	chr2:113671600-113683000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr2:113671800-113674600	Enhancers	Fetal Thymus	thymus
7	chr2:113671800-113675000	Enhancers	Thymus	Thymus
8	chr2:113672000-113672200	Enhancers	Spleen	Spleen
9	chr2:113672000-113674200	Enhancers	Primary T killer memory cells from peripheral blood	blood
10	chr2:113672000-113674600	Enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr2:113672200-113672400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr2:113672200-113674200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr2:113672400-113674200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr2:113672600-113677800	Enhancers	Fetal Intestine Small	intestine
15	chr2:113672800-113673200	Enhancers	Primary T cells from cord blood	blood
16	chr2:113672800-113673800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
17	chr2:113672800-113674000	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr2:113672800-113677600	Enhancers	Fetal Intestine Large	intestine
19	chr2:113673000-113673400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr2:113673000-113674200	Enhancers	Primary T helper cells fromperipheralblood	blood
21	chr2:113673200-113674000	Enhancers	GM12878-XiMat	blood
22	chr2:113674000-113674400	Flanking Active TSS	GM12878-XiMat	blood
23	chr2:113674200-113679400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr2:113674400-113674600	Enhancers	GM12878-XiMat	blood
25	chr2:113674400-113678400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr2:113674400-113683000	Weak transcription	Gastric	stomach
27	chr2:113674600-113674800	Bivalent Enhancer	GM12878-XiMat	blood
28	chr2:113674600-113678400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr2:113674800-113677000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr2:113674800-113678400	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr2:113676600-113676800	Enhancers	Thymus	Thymus
32	chr2:113676600-113677200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr2:113676800-113677000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
34	chr2:113676800-113677200	Enhancers	Stomach Mucosa	stomach
35	chr2:113677200-113679000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr2:113677200-113681800	Weak transcription	Stomach Mucosa	stomach
37	chr2:113677600-113678600	Weak transcription	Fetal Intestine Large	intestine
38	chr2:113677800-113678200	Weak transcription	Fetal Intestine Small	intestine
39	chr2:113678000-113679000	Enhancers	NHEK	skin
40	chr2:113678000-113679200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr2:113678200-113679000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr2:113678200-113679200	Enhancers	HMEC	breast
43	chr2:113678200-113683400	Enhancers	Fetal Intestine Small	intestine
44	chr2:113678400-113679000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr2:113678400-113679000	Enhancers	Primary T cells fromperipheralblood	blood
46	chr2:113678400-113679000	Enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr2:113678400-113679200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr2:113678600-113678800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr2:113678600-113678800	Enhancers	Brain Hippocampus Middle	brain
50	chr2:113678600-113678800	Enhancers	K562	blood

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