Variant report

Variant	nsv876298
Chromosome Location	chr3:610577-895346
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:837)
CpG islands
(count:61)
Chromatin interactive
region (count:30)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:888492-888519	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr3:892848-893082	GM12878	blood:	n/a	chr3:892988-892999
3	BATF	chr3:892892-893121	GM12878	blood:	n/a	chr3:892988-892999
4	BATF	chr3:638972-639242	GM12878	blood:	n/a	chr3:639093-639102
5	BHLHE40	chr3:846853-846863	GM12878	blood:	n/a	n/a
6	BRCA1	chr3:815996-816027	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr3:649451-649478	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr3:639591-639851	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr3:674381-674581	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr3:817416-817453	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr3:638578-639330	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr3:754720-755580	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr3:816945-817493	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr3:834255-834315	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr3:650039-650244	HepG2	liver:	n/a	chr3:650073-650084 chr3:650075-650084
16	CEBPB	chr3:780119-780347	HepG2	liver:	n/a	chr3:780198-780209
17	CEBPB	chr3:700997-701241	H1-hESC	embryonic stem cell:	n/a	chr3:701126-701139 chr3:701128-701137 chr3:701128-701137 chr3:701128-701137
18	CEBPB	chr3:701078-701278	A549	lung:	n/a	chr3:701126-701139 chr3:701128-701137 chr3:701128-701137 chr3:701128-701137
19	CEBPB	chr3:754295-754516	HepG2	liver:	n/a	chr3:754384-754393 chr3:754382-754393
20	CEBPB	chr3:754275-756263	Hela-S3	cervix:	n/a	chr3:754384-754393 chr3:754382-754393 chr3:755103-755114
21	CEBPB	chr3:780130-780267	K562	blood:	n/a	chr3:780198-780209
22	CEBPB	chr3:637765-638119	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr3:872412-872499	A549	lung:	n/a	n/a
24	CEBPB	chr3:766028-766169	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr3:649955-650248	IMR90	lung:	n/a	chr3:650073-650084 chr3:650075-650084
26	CEBPB	chr3:700968-701307	HepG2	liver:	n/a	chr3:701126-701139 chr3:701128-701137 chr3:701128-701137 chr3:701128-701137
27	CEBPB	chr3:611097-611344	HepG2	liver:	n/a	chr3:611201-611212
28	CEBPB	chr3:700965-701296	IMR90	lung:	n/a	chr3:701126-701139 chr3:701128-701137 chr3:701128-701137 chr3:701128-701137
29	CEBPB	chr3:746911-747209	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr3:672472-672697	A549	lung:	n/a	chr3:672554-672567 chr3:672555-672566
31	CEBPB	chr3:638934-639824	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr3:780178-780270	H1-hESC	embryonic stem cell:	n/a	chr3:780198-780209
33	CEBPB	chr3:674328-674574	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr3:766071-766268	HepG2	liver:	n/a	chr3:766173-766184
35	CEBPB	chr3:649124-649464	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr3:650024-650224	A549	lung:	n/a	chr3:650073-650084 chr3:650075-650084
37	CEBPB	chr3:700961-701300	Hela-S3	cervix:	n/a	chr3:701126-701139 chr3:701128-701137 chr3:701128-701137 chr3:701128-701137
38	CEBPB	chr3:775096-775429	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr3:879534-879816	A549	lung:	n/a	n/a
40	CEBPB	chr3:697395-697928	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr3:672488-672700	HepG2	liver:	n/a	chr3:672554-672567 chr3:672555-672566
42	CEBPB	chr3:795219-795424	K562	blood:	n/a	n/a
43	CHD1	chr3:894009-894041	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr3:660628-660658	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr3:639101-639345	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr3:754899-755419	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr3:834356-834507	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr3:893780-894020	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr3:674280-674430	HAc	cerebellar:	n/a	n/a
50	CTCF	chr3:893880-894030	HRE	kidney:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:782757-782807	AG09309	skin:	n/a
2	chr3:782757-782807	HCF	heart:	n/a
3	chr3:782757-782807	AoSMC	blood vessel:	n/a
4	chr3:782757-782807	ProgFib	skin:	n/a
5	chr3:782757-782807	SK-N-SH_RA	brain:	n/a
6	chr3:782757-782807	GM12878	blood:	n/a
7	chr3:782757-782807	SK-N-SH	brain:	n/a
8	chr3:782757-782807	GM06990	blood:	n/a
9	chr3:782757-782807	AG10803	skin:	n/a
10	chr3:782757-782807	NHDF-neo	bronchial:	n/a
11	chr3:782757-782807	HRPEpiC	eye:	n/a
12	chr3:782757-782807	HAEpiC	amniotic membrane:	n/a
13	chr3:782757-782807	ovcar-3	ovarian:	n/a
14	chr3:782757-782807	LNCaP	prostate:	n/a
15	chr3:782757-782807	HMEC	breast:	n/a
16	chr3:782757-782807	NH-A	brain:	n/a
17	chr3:782757-782807	CMK	blood:	n/a
18	chr3:782757-782807	GM12892	blood:	n/a
19	chr3:782757-782807	HL-60	blood:	n/a
20	chr3:782757-782807	IMR90	lung:	fetal
21	chr3:782757-782807	PrEC	prostate:	n/a
22	chr3:782757-782807	Jurkat	blood:	n/a
23	chr3:782757-782807	A549	lung:	n/a
24	chr3:782757-782807	Caco-2	colon:	n/a
25	chr3:782757-782807	HNPCEpiC	eye:	n/a
26	chr3:782757-782807	HPAEpiC	pulmonary alveolar:	n/a
27	chr3:782757-782807	GM19239	blood:	n/a
28	chr3:782757-782807	T-47D	breast:	n/a
29	chr3:782757-782807	PFSK-1	brain:	n/a
30	chr3:782757-782807	HCPEpiC	choroid plexus:	n/a
31	chr3:782757-782807	HEEpiC	esophagus:	n/a
32	chr3:782757-782807	NT2-D1	testis:	n/a
33	chr3:782757-782807	SK-N-MC	brain:	n/a
34	chr3:782757-782807	K562	blood:	n/a
35	chr3:782757-782807	HRCEpiC	kidney:	n/a
36	chr3:782757-782807	NHBE	bronchial:	n/a
37	chr3:782757-782807	HepG2	liver:	n/a
38	chr3:782757-782807	AG04450	lung:	fetal
39	chr3:782757-782807	PANC-1	pancreas:	n/a
40	chr3:782757-782807	H1-hESC	embryonic stem cell:	embryo
41	chr3:782757-782807	SAEC	small airway:	n/a
42	chr3:782757-782807	MCF-7	breast:	n/a
43	chr3:782757-782807	U87	brain:	n/a
44	chr3:782757-782807	AG04449	skin:	fetal
45	chr3:782757-782807	ECC-1	luminal epithelium:	n/a
46	chr3:782757-782807	AG09319	gingival:	n/a
47	chr3:782757-782807	MCF10A-Er-Src	breast:	n/a
48	chr3:782757-782807	HCT-116	colon:	n/a
49	chr3:782757-782807	NB4	blood:	n/a
50	chr3:782757-782807	RPTEC	kidney:	n/a

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No.	Distal block	Cell Line	Cell type
1	chr3:709932..711493-chr3:712317..715172,2	K562	blood:
2	chr1:229050784..229051693-chr3:758018..758663,2	MCF-7	breast:
3	chr12:101154422..101155178-chr3:753774..754622,2	MCF-7	breast:
4	chr3:746367..749271-chr3:749542..752426,2	K562	blood:
5	chr3:731301..733205-chr3:733252..736265,3	K562	blood:
6	chr3:731301..733205-chr3:733252..736265,3	K562	blood:
7	chr3:762317..764340-chr3:779905..782757,2	K562	blood:
8	chr3:703062..705164-chr3:828470..830008,2	K562	blood:
9	chr3:762317..764340-chr3:779905..782757,2	K562	blood:
10	chr3:751166..753010-chr3:765105..767568,2	K562	blood:
11	chr3:703062..705164-chr3:828470..830008,2	K562	blood:
12	chr21:9537493..9539688-chr3:612236..614804,2	MCF-7	breast:
13	chr3:726576..727076-chr3:11025934..11026463,2	MCF-7	breast:
14	chr3:746367..749271-chr3:749542..752426,2	K562	blood:
15	chr3:751166..753010-chr3:765105..767568,2	K562	blood:
16	chr21:9517250..9519290-chr3:632442..635070,2	MCF-7	breast:
17	chr3:674203..674975-chr3:2197712..2198482,2	MCF-7	breast:
18	chr3:805612..808013-chr3:811141..813375,2	K562	blood:
19	chr3:674217..674800-chr3:1123463..1123990,2	MCF-7	breast:
20	chr20:12921782..12922300-chr3:762237..762760,2	MCF-7	breast:
21	chr3:709932..711493-chr3:712317..715172,2	K562	blood:
22	chr21:9533639..9536328-chr3:614645..617390,2	MCF-7	breast:
23	chr3:829999..831597-chr3:832456..834541,2	MCF-7	breast:
24	chr3:805612..808013-chr3:811141..813375,2	K562	blood:
25	chr3:844122..846364-chr3:847958..849773,2	K562	blood:
26	chr3:522873..523625-chr3:674344..674995,2	MCF-7	breast:
27	chr3:829999..831597-chr3:832456..834541,2	MCF-7	breast:
28	chr3:844122..846364-chr3:847958..849773,2	K562	blood:
29	chr3:455533..456082-chr3:893341..894026,2	MCF-7	breast:
30	chr20:14175439..14177996-chr3:730394..733241,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHL1-3	chr3:884059-887698	NR_110118
2	lnc-CHL1-6	chr3:859059-862698	ucscGeneNc_uc003boy_1
3	lnc-CHL1-3	chr3:868690-868816	ENSG00000224957
4	lnc-CHL1-3	chr3:884059-884327	ENSG00000224957
5	lnc-CHL1-6	chr3:857398-857493	ucscGeneNc_uc003boy_1
6	lnc-CHL1-3	chr3:791898-791933	ENSG00000224957
7	lnc-CHL1-3	chr3:633788-633866	NR_110118
8	lnc-CHL1-3	chr3:882398-882493	NR_110118
9	lnc-IL5RA-14	chr3:659472-659997	NONHSAT087571
10	lnc-CHL1-3	chr3:791898-791933	NR_110118
11	lnc-CHL1-6	chr3:766898-766933	ucscGeneNc_uc003boy_1
12	lnc-CHL1-3	chr3:633788-633866	ENSG00000224957

No data

Variant related genes	Relation type
ENSG00000224239	TF binding region
ENSG00000238075	TF binding region
ENSG00000224239	CpG island
ENSG00000238075	CpG island
DCBLD2	miRNA target sites
COPS7A	miRNA target sites
IL10	miRNA target sites
HIF1A	miRNA target sites

Extended variants
information (count: 3216 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:3216 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2252871	chr3:610577-610578	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555709663	chr3:610604-610605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183085692	chr3:610619-610620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs544173593	chr3:610671-610672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556149013	chr3:610703-610704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs73095120	chr3:610729-610730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs74544540	chr3:610808-610809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs199928546	chr3:610821-610822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs559790689	chr3:610897-610898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs185721955	chr3:610902-610903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs190432398	chr3:610903-610904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs77253459	chr3:610921-610922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529639341	chr3:610928-610929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550971175	chr3:610968-610969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569269839	chr3:611001-611002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533141164	chr3:611016-611017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs182976269	chr3:611030-611031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs9834879	chr3:611032-611033	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs534277690	chr3:611042-611043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs374658221	chr3:611070-611071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187747018	chr3:611074-611075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79823039	chr3:611114-611115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538171889	chr3:611137-611138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556147901	chr3:611156-611157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs193140572	chr3:611166-611167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs544559479	chr3:611175-611176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553462323	chr3:611277-611278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571852836	chr3:611284-611285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs149880424	chr3:611307-611308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538477032	chr3:611312-611313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs529451176	chr3:611386-611387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147127619	chr3:611389-611390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182647463	chr3:611406-611407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187604276	chr3:611407-611408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs57567021	chr3:611422-611423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566868915	chr3:611479-611480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs73095121	chr3:611498-611499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558364124	chr3:611505-611506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192859898	chr3:611525-611526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184838746	chr3:611566-611567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560607723	chr3:611567-611568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188820192	chr3:611570-611571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73815304	chr3:611594-611595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs78432072	chr3:611623-611624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531308186	chr3:611664-611665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192078026	chr3:611697-611698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571685898	chr3:611709-611710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs535976963	chr3:611732-611733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554334935	chr3:611768-611769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs147951905	chr3:611801-611802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Cancer	20164920	CNVD
Lung cancer	16618734	CNVD
Autism	18349135	CNVD
Breast cancer	20409316	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Intellectual disability	22045946	CNVD
Squamous cell cancer	19607727	CNVD
Gastric adenocarcinoma	19115996	CNVD
sporadic birth defects	19047251	CNVD
Mental retardation	17124404	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Sudden cardiac death	19188705	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Neuroblastoma	18923191	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Autism	22543975	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Tetralogy of Fallot	22912587	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	20685689	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:608800-610600	Enhancers	Brain Germinal Matrix	brain
2	chr3:610000-611200	Enhancers	Fetal Brain Male	brain
3	chr3:610200-610600	Enhancers	Ovary	ovary
4	chr3:611200-612400	Weak transcription	Fetal Brain Male	brain
5	chr3:612600-612800	Enhancers	Fetal Brain Male	brain
6	chr3:636400-642600	Enhancers	Hela-S3	cervix
7	chr3:639200-639800	Enhancers	Dnd41	blood
8	chr3:649000-650000	Enhancers	Hela-S3	cervix
9	chr3:649200-650200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr3:659600-660000	Active TSS	Spleen	Spleen
11	chr3:663600-664000	Enhancers	Fetal Brain Male	brain
12	chr3:674200-674800	Enhancers	Brain Substantia Nigra	brain
13	chr3:674200-675000	Enhancers	Hela-S3	cervix
14	chr3:675800-676400	Enhancers	Fetal Thymus	thymus
15	chr3:682800-683200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr3:684800-685200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr3:697200-697600	Enhancers	Hela-S3	cervix
18	chr3:703200-703400	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr3:703400-703800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
20	chr3:706200-708000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr3:715600-716600	Enhancers	Fetal Brain Male	brain
22	chr3:716600-717800	Weak transcription	Fetal Brain Male	brain
23	chr3:718000-718200	Enhancers	Fetal Brain Male	brain
24	chr3:722800-723800	Enhancers	Hela-S3	cervix
25	chr3:723800-724400	Weak transcription	Hela-S3	cervix
26	chr3:724400-724600	Enhancers	Hela-S3	cervix
27	chr3:727000-727200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr3:729000-729400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr3:730600-732600	Weak transcription	Fetal Muscle Trunk	muscle
30	chr3:732000-732800	ZNF genes & repeats	Aorta	Aorta
31	chr3:732200-732400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr3:732200-732400	Weak transcription	Fetal Muscle Leg	muscle
33	chr3:732400-732800	ZNF genes & repeats	Lung	lung
34	chr3:732600-732800	Enhancers	Fetal Muscle Trunk	muscle
35	chr3:732800-734000	Weak transcription	Aorta	Aorta
36	chr3:742000-742400	Enhancers	Hela-S3	cervix
37	chr3:742200-742800	Enhancers	Fetal Muscle Leg	muscle
38	chr3:742400-743600	Flanking Active TSS	Hela-S3	cervix
39	chr3:743600-744000	Enhancers	Hela-S3	cervix
40	chr3:744200-756600	Weak transcription	Aorta	Aorta
41	chr3:746000-746200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr3:746400-747800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr3:747400-747600	Enhancers	Brain Hippocampus Middle	brain
44	chr3:747600-748200	Weak transcription	Brain Hippocampus Middle	brain
45	chr3:747800-750000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr3:748200-749600	Enhancers	Brain Hippocampus Middle	brain
47	chr3:748400-748800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr3:748400-748800	Enhancers	Brain Cingulate Gyrus	brain
49	chr3:748600-749000	Active TSS	Brain Substantia Nigra	brain
50	chr3:748600-749200	Enhancers	Brain Anterior Caudate	brain

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