Variant report

Variant	nsv582530
Chromosome Location	chr2:100739970-100774287
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:313)
CpG islands
(count:427)
Chromatin interactive
region (count:6)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:313 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr2:100758814-100759382	GM12878	blood:	n/a	n/a
2	ATF2	chr2:100747344-100747802	GM12878	blood:	n/a	n/a
3	ATF2	chr2:100752664-100753293	GM12878	blood:	n/a	n/a
4	ATF2	chr2:100752310-100753333	GM12878	blood:	n/a	n/a
5	ATF2	chr2:100758585-100759454	GM12878	blood:	n/a	n/a
6	BATF	chr2:100758807-100759336	GM12878	blood:	n/a	n/a
7	BATF	chr2:100758884-100759321	GM12878	blood:	n/a	n/a
8	BATF	chr2:100752314-100753166	GM12878	blood:	n/a	n/a
9	BATF	chr2:100751879-100752301	GM12878	blood:	n/a	n/a
10	BATF	chr2:100752739-100753152	GM12878	blood:	n/a	n/a
11	BATF	chr2:100747519-100747756	GM12878	blood:	n/a	n/a
12	BATF	chr2:100747403-100747828	GM12878	blood:	n/a	chr2:100747811-100747821
13	BCL11A	chr2:100752655-100753226	GM12878	blood:	n/a	n/a
14	BCL11A	chr2:100758988-100759232	GM12878	blood:	n/a	n/a
15	BCL11A	chr2:100758830-100759309	GM12878	blood:	n/a	n/a
16	BCL3	chr2:100752733-100753136	GM12878	blood:	n/a	n/a
17	BCL3	chr2:100758876-100759278	GM12878	blood:	n/a	n/a
18	BCL3	chr2:100752825-100753164	GM12878	blood:	n/a	n/a
19	BCL3	chr2:100758903-100759300	GM12878	blood:	n/a	n/a
20	BCLAF1	chr2:100752319-100753211	GM12878	blood:	n/a	n/a
21	BCLAF1	chr2:100758783-100759361	GM12878	blood:	n/a	n/a
22	BCLAF1	chr2:100758725-100759379	GM12878	blood:	n/a	n/a
23	BCLAF1	chr2:100747373-100747722	GM12878	blood:	n/a	n/a
24	BCLAF1	chr2:100752714-100753166	GM12878	blood:	n/a	n/a
25	BHLHE40	chr2:100758883-100759313	GM12878	blood:	n/a	n/a
26	BHLHE40	chr2:100753779-100754164	HepG2	liver:	n/a	n/a
27	BHLHE40	chr2:100752811-100753209	GM12878	blood:	n/a	n/a
28	CCNT2	chr2:100742029-100742224	K562	blood:	n/a	n/a
29	CEBPB	chr2:100752861-100753113	GM12878	blood:	n/a	n/a
30	CEBPB	chr2:100741288-100741647	Hela-S3	cervix:	n/a	chr2:100741312-100741323
31	CEBPB	chr2:100758940-100759267	GM12878	blood:	n/a	n/a
32	CEBPB	chr2:100753839-100754021	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:100752678-100753351	GM12878	blood:	n/a	n/a
34	CHD1	chr2:100759080-100759192	GM12878	blood:	n/a	n/a
35	CHD2	chr2:100758940-100759282	GM12878	blood:	n/a	n/a
36	CREB1	chr2:100758599-100759447	GM12878	blood:	n/a	n/a
37	CREB1	chr2:100752609-100753200	GM12878	blood:	n/a	n/a
38	CTCF	chr2:100758840-100758990	GM12871	blood:	n/a	n/a
39	CTCF	chr2:100758740-100758890	GM12874	blood:	n/a	n/a
40	CTCF	chr2:100758840-100758990	GM12872	blood:	n/a	n/a
41	CTCF	chr2:100742420-100742570	NHLF	lung:	n/a	n/a
42	CTCF	chr2:100758700-100758850	HL-60	blood:	n/a	n/a
43	CTCF	chr2:100758760-100758910	GM12865	blood:	n/a	n/a
44	CTCF	chr2:100755108-100755205	GM12891	blood:	n/a	n/a
45	CTCF	chr2:100758917-100758924	GM19240	blood:	n/a	n/a
46	CTCF	chr2:100758785-100758951	GM12892	blood:	n/a	n/a
47	CTCF	chr2:100758760-100758910	GM12875	blood:	n/a	n/a
48	CTCF	chr2:100758781-100758931	GM19238	blood:	n/a	n/a
49	CTCF	chr2:100758881-100758915	GM19240	blood:	n/a	n/a
50	CTCF	chr2:100763580-100763730	GM12875	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:100759159-100759209	HRPEpiC	eye:	n/a
2	chr2:100759623-100759673	NH-A	brain:	n/a
3	chr2:100759014-100759064	HMEC	breast:	n/a
4	chr2:100759159-100759209	NHBE	bronchial:	n/a
5	chr2:100759810-100759860	NHBE	bronchial:	n/a
6	chr2:100760351-100760401	MCF10A-Er-Src	breast:	n/a
7	chr2:100759845-100759895	ECC-1	luminal epithelium:	n/a
8	chr2:100759159-100759209	GM12878	blood:	n/a
9	chr2:100759623-100759673	HRPEpiC	eye:	n/a
10	chr2:100760351-100760401	H1-hESC	embryonic stem cell:	embryo
11	chr2:100760351-100760401	BE2_C	brain:	n/a
12	chr2:100759623-100759673	MCF-7	breast:	n/a
13	chr2:100759159-100759209	HAEpiC	amniotic membrane:	n/a
14	chr2:100760351-100760401	ProgFib	skin:	n/a
15	chr2:100759014-100759064	IMR90	lung:	fetal
16	chr2:100759014-100759064	MCF10A-Er-Src	breast:	n/a
17	chr2:100759845-100759895	MCF-7	breast:	n/a
18	chr2:100759810-100759860	SKMC	muscle:	n/a
19	chr2:100759845-100759895	NH-A	brain:	n/a
20	chr2:100759623-100759673	NHDF-neo	bronchial:	n/a
21	chr2:100759014-100759064	AG04449	skin:	fetal
22	chr2:100759623-100759673	HRCEpiC	kidney:	n/a
23	chr2:100759810-100759860	NB4	blood:	n/a
24	chr2:100760351-100760401	GM19239	blood:	n/a
25	chr2:100759810-100759860	SK-N-SH	brain:	n/a
26	chr2:100759845-100759895	GM06990	blood:	n/a
27	chr2:100759623-100759673	PANC-1	pancreas:	n/a
28	chr2:100759623-100759673	HL-60	blood:	n/a
29	chr2:100759845-100759895	AG09309	skin:	n/a
30	chr2:100759845-100759895	K562	blood:	n/a
31	chr2:100759810-100759860	ovcar-3	ovarian:	n/a
32	chr2:100759810-100759860	CMK	blood:	n/a
33	chr2:100759159-100759209	Jurkat	blood:	n/a
34	chr2:100759014-100759064	HepG2	liver:	n/a
35	chr2:100759134-100759184	HRE	kidney:	n/a
36	chr2:100759623-100759673	ovcar-3	ovarian:	n/a
37	chr2:100759810-100759860	HCT-116	colon:	n/a
38	chr2:100759014-100759064	SK-N-SH	brain:	n/a
39	chr2:100760351-100760401	HUVEC	blood vessel:	n/a
40	chr2:100759159-100759209	HCT-116	colon:	n/a
41	chr2:100759623-100759673	K562	blood:	n/a
42	chr2:100759159-100759209	ProgFib	skin:	n/a
43	chr2:100759014-100759064	AG10803	skin:	n/a
44	chr2:100759159-100759209	NB4	blood:	n/a
45	chr2:100759623-100759673	AG10803	skin:	n/a
46	chr2:100759623-100759673	NB4	blood:	n/a
47	chr2:100759810-100759860	U87	brain:	n/a
48	chr2:100759014-100759064	ProgFib	skin:	n/a
49	chr2:100759845-100759895	HL-60	blood:	n/a
50	chr2:100759014-100759064	AoSMC	blood vessel:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:100761253..100763849-chr2:100766044..100767965,2	K562	blood:
2	chr2:100740146..100742521-chr2:100744852..100747122,2	K562	blood:
3	chr2:100750345..100752144-chr2:100764723..100766529,2	MCF-7	breast:
4	chr2:100761253..100763849-chr2:100766044..100767965,2	K562	blood:
5	chr2:100740146..100742521-chr2:100744852..100747122,2	K562	blood:
6	chr2:100750345..100752144-chr2:100764723..100766529,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AFF3-1	chr2:100759173-100759201	NONHSAT072770
2	lnc-AFF3-1	chr2:100745686-100745768	NONHSAT072770
3	lnc-AFF3-1	chr2:100758946-100759057	NONHSAT072770

No data

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

Extended variants
information (count: 1033 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:1033 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6706188	chr2:100739970-100739971	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565416800	chr2:100739987-100739988	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs575938586	chr2:100740007-100740008	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs75305895	chr2:100740042-100740043	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs6748652	chr2:100740059-100740060	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs529714149	chr2:100740071-100740072	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs146002976	chr2:100740093-100740094	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560230677	chr2:100740157-100740158	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531994181	chr2:100740167-100740168	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552198843	chr2:100740168-100740169	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs569050395	chr2:100740176-100740177	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs184272528	chr2:100740194-100740195	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs548356523	chr2:100740230-100740231	Bivalent Enhancer Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190412080	chr2:100740252-100740253	Bivalent Enhancer Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs536708120	chr2:100740280-100740281	Bivalent Enhancer Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142164263	chr2:100740312-100740313	Bivalent Enhancer Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573345149	chr2:100740335-100740336	Bivalent Enhancer Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs371490956	chr2:100740369-100740370	Bivalent Enhancer Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs370894210	chr2:100740409-100740410	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs72238573	chr2:100740431-100740432	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531770031	chr2:100740508-100740509	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs62150260	chr2:100740520-100740521	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs573315668	chr2:100740562-100740563	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs558941170	chr2:100740578-100740579	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs538650930	chr2:100740589-100740590	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs368792717	chr2:100740622-100740623	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs374685999	chr2:100740626-100740627	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs151284785	chr2:100740644-100740645	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561112511	chr2:100740734-100740735	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574676799	chr2:100740757-100740758	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540456448	chr2:100740804-100740805	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs80049268	chr2:100740890-100740891	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs371735682	chr2:100740932-100740933	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs72966499	chr2:100740944-100740945	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181837148	chr2:100740946-100740947	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs72819177	chr2:100740949-100740950	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs562505683	chr2:100740995-100740996	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531607319	chr2:100740996-100740997	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184492308	chr2:100741013-100741014	Bivalent Enhancer Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574521548	chr2:100741039-100741040	Bivalent Enhancer Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs568396789	chr2:100741128-100741129	Bivalent Enhancer Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs368972748	chr2:100741135-100741136	Bivalent Enhancer Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs75176854	chr2:100741140-100741141	Bivalent Enhancer Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs188846268	chr2:100741167-100741168	Bivalent Enhancer Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs115126766	chr2:100741192-100741193	Bivalent Enhancer Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558654033	chr2:100741209-100741210	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559447987	chr2:100741246-100741247	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs139297865	chr2:100741277-100741278	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs6542913	chr2:100741327-100741328	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs554823695	chr2:100741374-100741375	Strong transcription ZNF genes & repeats Weak transcription Enhancers	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:311 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:100730200-100742200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr2:100730800-100746400	Weak transcription	Spleen	Spleen
3	chr2:100731800-100742000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr2:100732000-100749400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr2:100732000-100754400	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr2:100734400-100748000	Weak transcription	Adipose Nuclei	Adipose
7	chr2:100734600-100742200	Weak transcription	Pancreas	Pancrea
8	chr2:100735000-100741000	Strong transcription	Dnd41	blood
9	chr2:100735800-100744200	Strong transcription	Primary hematopoietic stem cells	blood
10	chr2:100736600-100742400	Strong transcription	Primary B cells from peripheral blood	blood
11	chr2:100736800-100740000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr2:100736800-100747400	Strong transcription	Primary B cells from cord blood	blood
13	chr2:100737400-100742200	Weak transcription	Thymus	Thymus
14	chr2:100738200-100741600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr2:100738200-100742400	Weak transcription	Fetal Thymus	thymus
16	chr2:100739600-100741400	ZNF genes & repeats	Primary T cells from cord blood	blood
17	chr2:100739600-100742400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr2:100739800-100746400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr2:100740000-100741200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr2:100740200-100740400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr2:100740200-100740400	Enhancers	Fetal Brain Male	brain
22	chr2:100740200-100740600	Enhancers	Placenta	Placenta
23	chr2:100740600-100740800	Weak transcription	Placenta	Placenta
24	chr2:100740800-100742000	Weak transcription	Fetal Brain Male	brain
25	chr2:100740800-100743000	Enhancers	Placenta	Placenta
26	chr2:100741000-100741200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr2:100741000-100742000	ZNF genes & repeats	Dnd41	blood
28	chr2:100741200-100745400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr2:100741400-100747000	Strong transcription	Primary T cells from cord blood	blood
30	chr2:100741600-100745800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
31	chr2:100742000-100742200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr2:100742000-100742800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr2:100742000-100743200	Enhancers	Brain Germinal Matrix	brain
34	chr2:100742000-100744000	Enhancers	Fetal Brain Male	brain
35	chr2:100742000-100744200	Enhancers	Fetal Heart	heart
36	chr2:100742000-100746000	Strong transcription	Dnd41	blood
37	chr2:100742200-100742400	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
38	chr2:100742200-100742400	Enhancers	Gastric	stomach
39	chr2:100742200-100742800	Enhancers	Pancreas	Pancrea
40	chr2:100742200-100742800	Enhancers	Right Ventricle	heart
41	chr2:100742200-100743000	Enhancers	Left Ventricle	heart
42	chr2:100742200-100743000	Enhancers	Right Atrium	heart
43	chr2:100742200-100743000	Strong transcription	Thymus	Thymus
44	chr2:100742200-100743600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr2:100742200-100747200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr2:100742400-100742800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr2:100742400-100743200	Strong transcription	Fetal Thymus	thymus
48	chr2:100742400-100743600	Genic enhancers	Primary B cells from peripheral blood	blood
49	chr2:100742400-100747200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr2:100742400-100753600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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