Variant report

Variant	nsv1003188
Chromosome Location	chr3:75427095-75674601
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2807)
CpG islands
(count:3233)
Chromatin interactive
region (count:9)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2807 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:75601426-75601483	K562	blood:	n/a	n/a
2	ARID3A	chr3:75482025-75482381	HepG2	liver:	n/a	n/a
3	ATF1	chr3:75482136-75482245	K562	blood:	n/a	n/a
4	ATF1	chr3:75484451-75484710	K562	blood:	n/a	n/a
5	ATF1	chr3:75442553-75442767	K562	blood:	n/a	n/a
6	ATF3	chr3:75482035-75482349	A549	lung:	n/a	n/a
7	ATF3	chr3:75482021-75482341	K562	blood:	n/a	n/a
8	BATF	chr3:75547955-75548333	GM12878	blood:	n/a	n/a
9	BATF	chr3:75551282-75551694	GM12878	blood:	n/a	n/a
10	BATF	chr3:75483065-75483278	GM12878	blood:	n/a	n/a
11	BATF	chr3:75566162-75566431	GM12878	blood:	n/a	n/a
12	BATF	chr3:75573541-75573863	GM12878	blood:	n/a	n/a
13	BATF	chr3:75653770-75654057	GM12878	blood:	n/a	n/a
14	BATF	chr3:75466554-75466845	GM12878	blood:	n/a	chr3:75466774-75466785
15	BATF	chr3:75573564-75573871	GM12878	blood:	n/a	n/a
16	BATF	chr3:75484448-75484647	GM12878	blood:	n/a	n/a
17	BATF	chr3:75467667-75467909	GM12878	blood:	n/a	n/a
18	BATF	chr3:75483500-75483898	GM12878	blood:	n/a	chr3:75483518-75483528 chr3:75483514-75483524
19	BATF	chr3:75468128-75468306	GM12878	blood:	n/a	n/a
20	BATF	chr3:75596078-75596520	GM12878	blood:	n/a	n/a
21	BATF	chr3:75551976-75552365	GM12878	blood:	n/a	n/a
22	BATF	chr3:75466555-75466915	GM12878	blood:	n/a	chr3:75466774-75466785
23	BATF	chr3:75471192-75471564	GM12878	blood:	n/a	n/a
24	BATF	chr3:75551286-75551692	GM12878	blood:	n/a	n/a
25	BATF	chr3:75478786-75479063	GM12878	blood:	n/a	n/a
26	BATF	chr3:75483970-75484356	GM12878	blood:	n/a	n/a
27	BATF	chr3:75653800-75653992	GM12878	blood:	n/a	n/a
28	BATF	chr3:75471237-75471503	GM12878	blood:	n/a	n/a
29	BATF	chr3:75544610-75544819	GM12878	blood:	n/a	chr3:75544723-75544731
30	BATF	chr3:75527612-75527941	GM12878	blood:	n/a	n/a
31	BATF	chr3:75483026-75483267	GM12878	blood:	n/a	n/a
32	BATF	chr3:75548046-75548331	GM12878	blood:	n/a	n/a
33	BCL11A	chr3:75466653-75466911	GM12878	blood:	n/a	chr3:75466778-75466787
34	BCL11A	chr3:75566204-75566463	GM12878	blood:	n/a	n/a
35	BCL11A	chr3:75544573-75544904	GM12878	blood:	n/a	chr3:75544808-75544817
36	BCL11A	chr3:75466632-75466905	GM12878	blood:	n/a	chr3:75466778-75466787
37	BCL11A	chr3:75467554-75467709	GM12878	blood:	n/a	n/a
38	BCL11A	chr3:75483447-75484322	GM12878	blood:	n/a	chr3:75483516-75483525
39	BCL11A	chr3:75547962-75548278	GM12878	blood:	n/a	n/a
40	BCL11A	chr3:75615329-75615521	GM12878	blood:	n/a	n/a
41	BCL11A	chr3:75547956-75548367	GM12878	blood:	n/a	chr3:75548358-75548367
42	BCL11A	chr3:75573652-75573882	GM12878	blood:	n/a	chr3:75573771-75573780
43	BCL11A	chr3:75551326-75551720	GM12878	blood:	n/a	n/a
44	BCL11A	chr3:75471159-75471563	GM12878	blood:	n/a	n/a
45	BCL11A	chr3:75609659-75609871	GM12878	blood:	n/a	n/a
46	BCL11A	chr3:75484021-75484296	GM12878	blood:	n/a	n/a
47	BCL11A	chr3:75527598-75527864	GM12878	blood:	n/a	n/a
48	BCL11A	chr3:75596331-75596513	GM12878	blood:	n/a	n/a
49	BCL11A	chr3:75483008-75483267	GM12878	blood:	n/a	n/a
50	BCL11A	chr3:75482472-75482657	GM12878	blood:	n/a	n/a

(count:3233 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75487529-75487579	MCF10A-Er-Src	breast:	n/a
2	chr3:75487529-75487579	HIPEpiC	eye:	n/a
3	chr3:75658490-75658540	HL-60	blood:	n/a
4	chr3:75443047-75443097	NT2-D1	testis:	n/a
5	chr3:75657183-75657233	PFSK-1	brain:	n/a
6	chr3:75484516-75484566	AG09309	skin:	n/a
7	chr3:75481281-75481331	CMK	blood:	n/a
8	chr3:75628932-75628982	SKMC	muscle:	n/a
9	chr3:75661320-75661370	AoSMC	blood vessel:	n/a
10	chr3:75555938-75555988	GM19239	blood:	n/a
11	chr3:75657183-75657233	ovcar-3	ovarian:	n/a
12	chr3:75631426-75631476	HCM	heart:	n/a
13	chr3:75658410-75658460	AG09309	skin:	n/a
14	chr3:75485110-75485160	PFSK-1	brain:	n/a
15	chr3:75668758-75668808	NHBE	bronchial:	n/a
16	chr3:75631426-75631476	PFSK-1	brain:	n/a
17	chr3:75485110-75485160	U87	brain:	n/a
18	chr3:75441804-75441854	PANC-1	pancreas:	n/a
19	chr3:75484213-75484263	SKMC	muscle:	n/a
20	chr3:75444752-75444802	HepG2	liver:	n/a
21	chr3:75653319-75653369	NHBE	bronchial:	n/a
22	chr3:75653319-75653369	HepG2	liver:	n/a
23	chr3:75666381-75666431	PANC-1	pancreas:	n/a
24	chr3:75657758-75657808	GM12892	blood:	n/a
25	chr3:75482182-75482232	HMEC	breast:	n/a
26	chr3:75628819-75628869	HepG2	liver:	n/a
27	chr3:75445610-75445660	GM12891	blood:	n/a
28	chr3:75658490-75658540	GM12892	blood:	n/a
29	chr3:75487529-75487579	HCM	heart:	n/a
30	chr3:75628819-75628869	AG04450	lung:	fetal
31	chr3:75664059-75664109	Hepatocyte	liver:	n/a
32	chr3:75484209-75484259	BE2_C	brain:	n/a
33	chr3:75628819-75628869	A549	lung:	n/a
34	chr3:75445610-75445660	NHBE	bronchial:	n/a
35	chr3:75631426-75631476	HRPEpiC	eye:	n/a
36	chr3:75668627-75668677	BE2_C	brain:	n/a
37	chr3:75441804-75441854	NH-A	brain:	n/a
38	chr3:75658490-75658540	ECC-1	luminal epithelium:	n/a
39	chr3:75671115-75671165	AG04449	skin:	fetal
40	chr3:75631426-75631476	BE2_C	brain:	n/a
41	chr3:75443047-75443097	HRPEpiC	eye:	n/a
42	chr3:75668627-75668677	K562	blood:	n/a
43	chr3:75628932-75628982	HUVEC	blood vessel:	n/a
44	chr3:75659629-75659679	AG04449	skin:	fetal
45	chr3:75629039-75629089	HCM	heart:	n/a
46	chr3:75553762-75553812	Hela-S3	cervix:	n/a
47	chr3:75658410-75658460	NHBE	bronchial:	n/a
48	chr3:75664059-75664109	Jurkat	blood:	n/a
49	chr3:75659629-75659679	SKMC	muscle:	n/a
50	chr3:75553294-75553344	U87	brain:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:71498107..71498639-chr3:75483883..75484386,2	Hela-S3	cervix:
2	chr3:75343239..75343917-chr3:75478470..75479360,2	MCF-7	breast:
3	chr3:75343052..75344300-chr3:75470848..75471840,6	MCF-7	breast:
4	chr16:436504..437180-chr3:75674246..75674764,2	MCF-7	breast:
5	chr3:75343397..75343923-chr3:75600934..75601577,2	MCF-7	breast:
6	chr3:75390707..75391392-chr3:75471007..75471537,3	MCF-7	breast:
7	chr3:75466672..75467412-chr3:129812592..129813394,2	NB4	blood:
8	chr3:75484863..75485638-chr6:26156199..26156944,2	HCT-116	colon:
9	chr3:75343035..75343810-chr3:75470999..75471871,7	MCF-7	breast:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG2C-3	chr3:75488905-75488997	XLOC_002710
2	lnc-FRG2C-3	chr3:75496316-75496447	ENSG00000272690.1
3	lnc-ZNF717-3	chr3:75589200-75589378	ENSG00000272710.1
4	lnc-FRG2C-3	chr3:75485928-75486426	XLOC_002710
5	lnc-FRG2C-3	chr3:75492659-75492797	ENSG00000272690.1
6	lnc-FRG2C-2	chr3:75608026-75608398	XLOC_002712
7	lnc-FRG2C-11	chr3:75570954-75571163	NONHSAT090534
8	lnc-FRG2C-3	chr3:75500361-75500553	ENSG00000272690.1
9	lnc-FRG2C-3	chr3:75484499-75484564	ENSG00000272690.1
10	lnc-FRG2C-2	chr3:75606117-75606146	XLOC_002712
11	lnc-FRG2C-3	chr3:75501348-75501809	ENSG00000272690.1
12	lnc-FRG2C-3	chr3:75500361-75500553	ENSG00000272690.1
13	lnc-ZNF717-1	chr3:75674122-75674304	NONHSAT090540
14	lnc-FRG2C-3	chr3:75501683-75501802	ENSG00000272690.1
15	lnc-FRG2C-3	chr3:75497520-75500553	NONHSAT090533
16	lnc-FRG2C-3	chr3:75486207-75486426	XLOC_002710
17	lnc-FRG2C-3	chr3:75505768-75506637	ENSG00000272690.1
18	lnc-FRG2C-2	chr3:75606223-75606260	XLOC_002712
19	lnc-FRG2C-3	chr3:75501683-75501794	NONHSAT090533
20	lnc-ZNF717-3	chr3:75629129-75629150	ENSG00000272710.1
21	lnc-FRG2C-3	chr3:75492659-75492775	XLOC_002710
22	lnc-FRG2C-2	chr3:75608026-75608433	XLOC_002712
23	lnc-FRG2C-3	chr3:75485367-75485503	XLOC_002710
24	lnc-FRG2C-3	chr3:75488905-75488988	XLOC_002710

No data

Variant related genes	Relation type
UNC93B3	TF binding region
ENSG00000243422	TF binding region
ENSG00000239383	TF binding region
RPS3AP15	TF binding region
ENSG00000243794	TF binding region
OR7E121P	TF binding region
ENSG00000272690	TF binding region
FAM86DP	TF binding region
ENSG00000242953	TF binding region
ENSG00000221602	TF binding region
LSP1P2	TF binding region
ENPP7P2	TF binding region
ALG1L6P	TF binding region
ENSG00000244699	TF binding region
ENSG00000272710	TF binding region
UNC93B3	CpG island
ENSG00000243422	CpG island
ENSG00000239383	CpG island
RPS3AP15	CpG island
ENSG00000243794	CpG island
OR7E121P	CpG island
ENSG00000272690	CpG island
FAM86DP	CpG island
ENSG00000242953	CpG island
ENSG00000221602	CpG island
LSP1P2	CpG island
ENPP7P2	CpG island
ALG1L6P	CpG island
ENSG00000244699	CpG island
ENSG00000272710	CpG island
ENSG00000248243	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000129925	chromatin interactions
ENSG00000251287	chromatin interactions
ENSG00000236829	chromatin interactions
ENSG00000158483	chromatin interactions
ITGB1	miRNA target sites
SFRS5	miRNA target sites

Extended variants
information (count: 9468 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:9468 , 50 per page) page: 1 2 3 4 5 6 7 ... 190

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563883060	chr3:75427601-75427602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs186439026	chr3:75427622-75427623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs546335922	chr3:75427634-75427635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs568047646	chr3:75427686-75427687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532343975	chr3:75427740-75427741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567339997	chr3:75427750-75427751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs550909030	chr3:75427806-75427807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs569155983	chr3:75427811-75427812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs148586225	chr3:75427856-75427857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs146558067	chr3:75427861-75427862	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369607561	chr3:75427873-75427874	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs534237720	chr3:75427905-75427906	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs535128976	chr3:75428006-75428007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553146071	chr3:75428009-75428010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs146620895	chr3:75428038-75428039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546267692	chr3:75428040-75428041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189869006	chr3:75428079-75428080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs557268738	chr3:75428093-75428094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs373543214	chr3:75428123-75428124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs575512541	chr3:75428152-75428153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs546026908	chr3:75428206-75428207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs116425842	chr3:75428217-75428218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528629235	chr3:75428224-75428225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540342502	chr3:75428251-75428252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs140066382	chr3:75428258-75428259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs17028317	chr3:75428271-75428272	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs550572394	chr3:75428279-75428280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569541579	chr3:75428337-75428338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182131026	chr3:75428347-75428348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533255632	chr3:75428374-75428375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551660947	chr3:75428388-75428389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538145719	chr3:75428393-75428394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374539695	chr3:75428401-75428402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192001223	chr3:75428417-75428418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547088915	chr3:75428421-75428422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568448966	chr3:75428422-75428423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188332526	chr3:75428426-75428427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs377082927	chr3:75428460-75428461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556925575	chr3:75428490-75428491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575195105	chr3:75428491-75428492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539744689	chr3:75428495-75428496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191062155	chr3:75428511-75428512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183174433	chr3:75428514-75428515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116067763	chr3:75428560-75428561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs17028321	chr3:75428568-75428569	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs116590427	chr3:75428578-75428579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73116942	chr3:75428579-75428580	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs143736697	chr3:75428590-75428591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532910125	chr3:75428596-75428597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188503746	chr3:75428609-75428610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	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
Oral squamous cell carcinoma	17134496	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
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Autism	22102821	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Melanoma	20877625	CNVD
Ollier disease	21235737	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:1797 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75427600-75427800	Enhancers	Fetal Lung	lung
2	chr3:75427800-75428000	Enhancers	Fetal Heart	heart
3	chr3:75427800-75428200	Enhancers	Fetal Muscle Leg	muscle
4	chr3:75427800-75429000	Weak transcription	Fetal Lung	lung
5	chr3:75428000-75429000	Weak transcription	Fetal Heart	heart
6	chr3:75429000-75429200	Enhancers	Fetal Lung	lung
7	chr3:75429000-75429600	Enhancers	Fetal Heart	heart
8	chr3:75429000-75429600	Enhancers	Gastric	stomach
9	chr3:75429000-75429800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr3:75429000-75429800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr3:75429000-75429800	ZNF genes & repeats	Fetal Kidney	kidney
12	chr3:75429000-75429800	Enhancers	Pancreas	Pancrea
13	chr3:75429200-75429800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr3:75429200-75429800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr3:75429200-75429800	Active TSS	Fetal Lung	lung
16	chr3:75429200-75429800	ZNF genes & repeats	Dnd41	blood
17	chr3:75429400-75429800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr3:75429600-75429800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr3:75429800-75430200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr3:75429800-75445600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr3:75430000-75430200	Weak transcription	Fetal Kidney	kidney
22	chr3:75431600-75431800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:75431800-75432600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr3:75432000-75432200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr3:75432200-75433000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr3:75432600-75432800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr3:75432600-75433000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr3:75432800-75433400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:75435800-75436000	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr3:75435800-75436400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr3:75436400-75437400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr3:75437400-75437600	Enhancers	Muscle Satellite Cultured Cells	--
33	chr3:75437400-75437600	Enhancers	Osteobl	bone
34	chr3:75437400-75437800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr3:75437400-75438200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr3:75437400-75438200	Enhancers	Ovary	ovary
37	chr3:75437400-75438200	Enhancers	Right Atrium	heart
38	chr3:75437400-75438400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr3:75437400-75438400	Enhancers	Rectal Smooth Muscle	rectum
40	chr3:75437400-75438800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr3:75437400-75439000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr3:75437600-75438000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
43	chr3:75437600-75438000	Flanking Active TSS	Osteobl	bone
44	chr3:75437600-75438200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr3:75437600-75438200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr3:75437600-75438800	Enhancers	NH-A	brain
47	chr3:75437600-75442000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr3:75437800-75438200	Enhancers	Colon Smooth Muscle	Colon
49	chr3:75437800-75438200	Enhancers	Duodenum Smooth Muscle	Duodenum
50	chr3:75437800-75438200	Enhancers	Fetal Muscle Trunk	muscle

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