Variant report

Variant	nsv527481
Chromosome Location	chr2:100753490-100763006
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:171)
CpG islands
(count:428)
Chromatin interactive
region (count:1)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:171 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr2:100758585-100759454	GM12878	blood:	n/a	n/a
2	ATF2	chr2:100758814-100759382	GM12878	blood:	n/a	n/a
3	BATF	chr2:100758884-100759321	GM12878	blood:	n/a	n/a
4	BATF	chr2:100758807-100759336	GM12878	blood:	n/a	n/a
5	BCL11A	chr2:100758830-100759309	GM12878	blood:	n/a	n/a
6	BCL11A	chr2:100758988-100759232	GM12878	blood:	n/a	n/a
7	BCL3	chr2:100758876-100759278	GM12878	blood:	n/a	n/a
8	BCL3	chr2:100758903-100759300	GM12878	blood:	n/a	n/a
9	BCLAF1	chr2:100758783-100759361	GM12878	blood:	n/a	n/a
10	BCLAF1	chr2:100758725-100759379	GM12878	blood:	n/a	n/a
11	BHLHE40	chr2:100753779-100754164	HepG2	liver:	n/a	n/a
12	BHLHE40	chr2:100758883-100759313	GM12878	blood:	n/a	n/a
13	CEBPB	chr2:100753839-100754021	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:100758940-100759267	GM12878	blood:	n/a	n/a
15	CHD1	chr2:100759080-100759192	GM12878	blood:	n/a	n/a
16	CHD2	chr2:100758940-100759282	GM12878	blood:	n/a	n/a
17	CREB1	chr2:100758599-100759447	GM12878	blood:	n/a	n/a
18	CTCF	chr2:100758760-100758910	GM12875	blood:	n/a	n/a
19	CTCF	chr2:100758740-100758890	GM12874	blood:	n/a	n/a
20	CTCF	chr2:100758420-100758570	GM12875	blood:	n/a	n/a
21	CTCF	chr2:100758700-100758850	HL-60	blood:	n/a	n/a
22	CTCF	chr2:100758881-100758915	GM19240	blood:	n/a	n/a
23	CTCF	chr2:100758760-100758910	GM12865	blood:	n/a	n/a
24	CTCF	chr2:100758840-100758990	GM12872	blood:	n/a	n/a
25	CTCF	chr2:100759040-100759190	GM12873	blood:	n/a	n/a
26	CTCF	chr2:100755108-100755205	GM12891	blood:	n/a	n/a
27	CTCF	chr2:100758820-100758970	GM12873	blood:	n/a	n/a
28	CTCF	chr2:100758860-100759010	GM12872	blood:	n/a	n/a
29	CTCF	chr2:100758840-100758990	GM12871	blood:	n/a	n/a
30	CTCF	chr2:100758785-100758951	GM12892	blood:	n/a	n/a
31	CTCF	chr2:100758781-100758931	GM19238	blood:	n/a	n/a
32	CTCF	chr2:100758917-100758924	GM19240	blood:	n/a	n/a
33	CTCF	chr2:100758920-100759070	GM12873	blood:	n/a	n/a
34	CTCF	chr2:100758775-100758927	GM12891	blood:	n/a	n/a
35	EBF1	chr2:100758987-100759265	GM12878	blood:	n/a	n/a
36	EBF1	chr2:100758849-100759316	GM12878	blood:	n/a	n/a
37	EBF1	chr2:100758934-100759320	GM12878	blood:	n/a	n/a
38	EGR1	chr2:100758970-100759280	GM12878	blood:	n/a	n/a
39	EGR1	chr2:100758946-100759254	GM12878	blood:	n/a	n/a
40	ELF1	chr2:100758903-100759406	GM12878	blood:	n/a	n/a
41	ELF1	chr2:100758947-100759300	GM12878	blood:	n/a	n/a
42	ELK1	chr2:100758959-100759282	GM12878	blood:	n/a	n/a
43	EP300	chr2:100758849-100759349	GM12878	blood:	n/a	chr2:100759110-100759124
44	EP300	chr2:100758938-100759312	GM12878	blood:	n/a	chr2:100759110-100759124
45	EP300	chr2:100759004-100759251	GM12878	blood:	n/a	chr2:100759110-100759124
46	EP300	chr2:100758905-100759536	GM12878	blood:	n/a	chr2:100759110-100759124
47	EP300	chr2:100755560-100755980	SK-N-SH_RA	brain:	n/a	n/a
48	EP300	chr2:100754324-100754569	SK-N-SH_RA	brain:	n/a	n/a
49	EP300	chr2:100755570-100756112	SK-N-SH_RA	brain:	n/a	n/a
50	EP300	chr2:100753460-100756870	SK-N-SH	brain:	n/a	chr2:100756503-100756517 chr2:100756239-100756253 chr2:100754674-100754681

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:100759014-100759064	SK-N-SH	brain:	n/a
2	chr2:100759014-100759064	SK-N-SH	brain:	n/a
3	chr2:100760351-100760401	U87	brain:	n/a
4	chr2:100760351-100760401	AG04449	skin:	fetal
5	chr2:100759159-100759209	MCF-7	breast:	n/a
6	chr2:100759134-100759184	HRCEpiC	kidney:	n/a
7	chr2:100759845-100759895	HepG2	liver:	n/a
8	chr2:100759014-100759064	Hela-S3	cervix:	n/a
9	chr2:100759159-100759209	Hepatocyte	liver:	n/a
10	chr2:100759845-100759895	NHBE	bronchial:	n/a
11	chr2:100759159-100759209	GM06990	blood:	n/a
12	chr2:100759134-100759184	MCF10A-Er-Src	breast:	n/a
13	chr2:100759810-100759860	NHBE	bronchial:	n/a
14	chr2:100759623-100759673	Caco-2	colon:	n/a
15	chr2:100759134-100759184	HCT-116	colon:	n/a
16	chr2:100759134-100759184	HEK293	kidney:	embryo
17	chr2:100759134-100759184	ProgFib	skin:	n/a
18	chr2:100759014-100759064	AoSMC	blood vessel:	n/a
19	chr2:100759014-100759064	ProgFib	skin:	n/a
20	chr2:100759134-100759184	HUVEC	blood vessel:	n/a
21	chr2:100759134-100759184	T-47D	breast:	n/a
22	chr2:100759014-100759064	BJ	skin:	n/a
23	chr2:100759159-100759209	AG09309	skin:	n/a
24	chr2:100759623-100759673	ProgFib	skin:	n/a
25	chr2:100760351-100760401	Hepatocyte	liver:	n/a
26	chr2:100759845-100759895	PFSK-1	brain:	n/a
27	chr2:100759845-100759895	HCPEpiC	choroid plexus:	n/a
28	chr2:100760351-100760401	ovcar-3	ovarian:	n/a
29	chr2:100759810-100759860	HL-60	blood:	n/a
30	chr2:100760351-100760401	NHDF-neo	bronchial:	n/a
31	chr2:100759159-100759209	HMEC	breast:	n/a
32	chr2:100759810-100759860	MCF-7	breast:	n/a
33	chr2:100759014-100759064	HPAEpiC	pulmonary alveolar:	n/a
34	chr2:100760351-100760401	HIPEpiC	eye:	n/a
35	chr2:100760351-100760401	GM19239	blood:	n/a
36	chr2:100759159-100759209	CMK	blood:	n/a
37	chr2:100760351-100760401	BJ	skin:	n/a
38	chr2:100759623-100759673	HL-60	blood:	n/a
39	chr2:100759134-100759184	NB4	blood:	n/a
40	chr2:100759014-100759064	PFSK-1	brain:	n/a
41	chr2:100759845-100759895	ovcar-3	ovarian:	n/a
42	chr2:100759845-100759895	PANC-1	pancreas:	n/a
43	chr2:100759134-100759184	K562	blood:	n/a
44	chr2:100760351-100760401	GM12892	blood:	n/a
45	chr2:100759134-100759184	BJ	skin:	n/a
46	chr2:100760351-100760401	SK-N-MC	brain:	n/a
47	chr2:100760351-100760401	RPTEC	kidney:	n/a
48	chr2:100760351-100760401	SAEC	small airway:	n/a
49	chr2:100759810-100759860	HEEpiC	esophagus:	n/a
50	chr2:100759810-100759860	NHDF-neo	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:100761253..100763849-chr2:100766044..100767965,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AFF3-1	chr2:100758946-100759057	NONHSAT072770
2	lnc-AFF3-1	chr2:100759173-100759201	NONHSAT072770

No data

Variant related genes	Relation type
AFF3	TF binding region
AFF3	CpG island

Extended variants
information (count: 397 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:397 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4851251	chr2:100753490-100753491	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs148904929	chr2:100753511-100753512	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs529691103	chr2:100753543-100753544	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs190290147	chr2:100753550-100753551	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs78554881	chr2:100753562-100753563	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181108416	chr2:100753583-100753584	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs57426399	chr2:100753584-100753585	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs552407450	chr2:100753586-100753587	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs76396728	chr2:100753602-100753603	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs185203447	chr2:100753654-100753655	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs535301385	chr2:100753655-100753656	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs553987686	chr2:100753738-100753739	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs537562104	chr2:100753847-100753848	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs13000759	chr2:100753903-100753904	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs13019618	chr2:100753963-100753964	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs148058424	chr2:100753971-100753972	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs72819181	chr2:100753984-100753985	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs143666386	chr2:100753985-100753986	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs138627904	chr2:100753998-100753999	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs113672325	chr2:100754015-100754016	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs545158613	chr2:100754020-100754021	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs3038476	chr2:100754021-100754022	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs62150272	chr2:100754022-100754023	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs70940196	chr2:100754024-100754025	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs201023304	chr2:100754070-100754071	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs73966422	chr2:100754089-100754090	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs35267826	chr2:100754093-100754094	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs147187723	chr2:100754111-100754112	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs191085280	chr2:100754127-100754128	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs529688442	chr2:100754182-100754183	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs558626498	chr2:100754204-100754205	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs560446090	chr2:100754213-100754214	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs532448752	chr2:100754224-100754225	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs139168301	chr2:100754287-100754288	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs117249332	chr2:100754395-100754396	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs113409417	chr2:100754436-100754437	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs558993315	chr2:100754440-100754441	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs551034383	chr2:100754449-100754450	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs373753376	chr2:100754519-100754520	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs567703442	chr2:100754520-100754521	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs115447873	chr2:100754531-100754532	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs143073622	chr2:100754533-100754534	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs566778622	chr2:100754617-100754618	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
44	rs538968632	chr2:100754618-100754619	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
45	rs139228874	chr2:100754638-100754639	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
46	rs575411096	chr2:100754642-100754643	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
47	rs538102832	chr2:100754666-100754667	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
48	rs576892942	chr2:100754720-100754721	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
49	rs574457362	chr2:100754743-100754744	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
50	rs544301547	chr2:100754863-100754864	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

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
Medulloblastoma	20607354	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
Ovarian cancer	21781307	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
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:191 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:100732000-100754400	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr2:100742400-100753600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr2:100742400-100754000	Weak transcription	Gastric	stomach
4	chr2:100742800-100754000	Weak transcription	Lung	lung
5	chr2:100746200-100764800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr2:100747000-100753800	Weak transcription	Thymus	Thymus
7	chr2:100747200-100758400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr2:100750200-100754000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr2:100751000-100753600	Genic enhancers	Primary B cells from cord blood	blood
10	chr2:100751200-100754000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr2:100751200-100754400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr2:100751200-100755400	Genic enhancers	Primary B cells from peripheral blood	blood
13	chr2:100751400-100757000	Enhancers	Primary hematopoietic stem cells	blood
14	chr2:100751600-100756600	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr2:100752400-100753600	Weak transcription	Fetal Thymus	thymus
16	chr2:100752600-100753600	Enhancers	GM12878-XiMat	blood
17	chr2:100752600-100758200	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr2:100752800-100753800	Enhancers	Dnd41	blood
19	chr2:100753000-100754400	Enhancers	Primary T cells from cord blood	blood
20	chr2:100753000-100758400	Weak transcription	Spleen	Spleen
21	chr2:100753600-100754400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr2:100753600-100754600	Bivalent Enhancer	GM12878-XiMat	blood
23	chr2:100753600-100755000	Transcr. at gene 5' and 3'	Primary B cells from cord blood	blood
24	chr2:100753600-100756000	Enhancers	Primary T helper cells PMA-I stimulated	--
25	chr2:100753600-100756000	Enhancers	Fetal Thymus	thymus
26	chr2:100753600-100757800	Enhancers	Primary T killer memory cells from peripheral blood	blood
27	chr2:100753600-100758200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr2:100753800-100755000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr2:100753800-100755600	Enhancers	Primary T cells fromperipheralblood	blood
30	chr2:100753800-100756200	Enhancers	Thymus	Thymus
31	chr2:100753800-100757800	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr2:100753800-100759800	Flanking Active TSS	Dnd41	blood
33	chr2:100754000-100754600	Enhancers	Gastric	stomach
34	chr2:100754000-100754800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
35	chr2:100754000-100754800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr2:100754000-100754800	Enhancers	Lung	lung
37	chr2:100754000-100755000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr2:100754000-100758200	Enhancers	Primary T helper naive cells from peripheral blood	blood
39	chr2:100754200-100754600	Enhancers	Sigmoid Colon	Sigmoid Colon
40	chr2:100754200-100754800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr2:100754400-100754600	Flanking Active TSS	Primary T cells from cord blood	blood
42	chr2:100754400-100754800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr2:100754400-100754800	Enhancers	Brain Germinal Matrix	brain
44	chr2:100754400-100758400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
45	chr2:100754400-100758400	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr2:100754600-100754800	Enhancers	Primary T cells from cord blood	blood
47	chr2:100754600-100754800	Flanking Bivalent TSS/Enh	GM12878-XiMat	blood
48	chr2:100754800-100755000	Flanking Active TSS	Primary T cells from cord blood	blood
49	chr2:100754800-100755000	Bivalent Enhancer	GM12878-XiMat	blood
50	chr2:100754800-100756800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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