Variant report

Variant	nsv1002268
Chromosome Location	chr3:75406386-75586793
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2145)
CpG islands
(count:2261)
Chromatin interactive
region (count:7)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2145 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:75482025-75482381	HepG2	liver:	n/a	n/a
2	ATF1	chr3:75482136-75482245	K562	blood:	n/a	n/a
3	ATF1	chr3:75484451-75484710	K562	blood:	n/a	n/a
4	ATF1	chr3:75442553-75442767	K562	blood:	n/a	n/a
5	ATF3	chr3:75482021-75482341	K562	blood:	n/a	n/a
6	ATF3	chr3:75482035-75482349	A549	lung:	n/a	n/a
7	BATF	chr3:75466555-75466915	GM12878	blood:	n/a	chr3:75466774-75466785
8	BATF	chr3:75551976-75552365	GM12878	blood:	n/a	n/a
9	BATF	chr3:75483026-75483267	GM12878	blood:	n/a	n/a
10	BATF	chr3:75468128-75468306	GM12878	blood:	n/a	n/a
11	BATF	chr3:75551286-75551692	GM12878	blood:	n/a	n/a
12	BATF	chr3:75573564-75573871	GM12878	blood:	n/a	n/a
13	BATF	chr3:75466554-75466845	GM12878	blood:	n/a	chr3:75466774-75466785
14	BATF	chr3:75544610-75544819	GM12878	blood:	n/a	chr3:75544723-75544731
15	BATF	chr3:75467667-75467909	GM12878	blood:	n/a	n/a
16	BATF	chr3:75471192-75471564	GM12878	blood:	n/a	n/a
17	BATF	chr3:75411520-75411813	GM12878	blood:	n/a	n/a
18	BATF	chr3:75548046-75548331	GM12878	blood:	n/a	n/a
19	BATF	chr3:75471237-75471503	GM12878	blood:	n/a	n/a
20	BATF	chr3:75551282-75551694	GM12878	blood:	n/a	n/a
21	BATF	chr3:75547955-75548333	GM12878	blood:	n/a	n/a
22	BATF	chr3:75527612-75527941	GM12878	blood:	n/a	n/a
23	BATF	chr3:75573541-75573863	GM12878	blood:	n/a	n/a
24	BATF	chr3:75484448-75484647	GM12878	blood:	n/a	n/a
25	BATF	chr3:75483970-75484356	GM12878	blood:	n/a	n/a
26	BATF	chr3:75478786-75479063	GM12878	blood:	n/a	n/a
27	BATF	chr3:75483065-75483278	GM12878	blood:	n/a	n/a
28	BATF	chr3:75483500-75483898	GM12878	blood:	n/a	chr3:75483518-75483528 chr3:75483514-75483524
29	BATF	chr3:75566162-75566431	GM12878	blood:	n/a	n/a
30	BATF	chr3:75411604-75411874	GM12878	blood:	n/a	n/a
31	BCL11A	chr3:75527598-75527864	GM12878	blood:	n/a	n/a
32	BCL11A	chr3:75547962-75548278	GM12878	blood:	n/a	n/a
33	BCL11A	chr3:75483008-75483267	GM12878	blood:	n/a	n/a
34	BCL11A	chr3:75466653-75466911	GM12878	blood:	n/a	chr3:75466778-75466787
35	BCL11A	chr3:75467554-75467709	GM12878	blood:	n/a	n/a
36	BCL11A	chr3:75551326-75551720	GM12878	blood:	n/a	n/a
37	BCL11A	chr3:75471159-75471563	GM12878	blood:	n/a	n/a
38	BCL11A	chr3:75483449-75483810	GM12878	blood:	n/a	chr3:75483516-75483525
39	BCL11A	chr3:75566204-75566463	GM12878	blood:	n/a	n/a
40	BCL11A	chr3:75544573-75544904	GM12878	blood:	n/a	chr3:75544808-75544817
41	BCL11A	chr3:75466632-75466905	GM12878	blood:	n/a	chr3:75466778-75466787
42	BCL11A	chr3:75547956-75548367	GM12878	blood:	n/a	chr3:75548358-75548367
43	BCL11A	chr3:75482472-75482657	GM12878	blood:	n/a	n/a
44	BCL11A	chr3:75471268-75471550	GM12878	blood:	n/a	n/a
45	BCL11A	chr3:75484021-75484296	GM12878	blood:	n/a	n/a
46	BCL11A	chr3:75551437-75551623	GM12878	blood:	n/a	n/a
47	BCL11A	chr3:75573652-75573882	GM12878	blood:	n/a	chr3:75573771-75573780
48	BCL11A	chr3:75483447-75484322	GM12878	blood:	n/a	chr3:75483516-75483525
49	BCL3	chr3:75417298-75417641	GM12878	blood:	n/a	n/a
50	BCL3	chr3:75416737-75417040	GM12878	blood:	n/a	n/a

(count:2261 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75411217-75411267	Jurkat	blood:	n/a
2	chr3:75484516-75484566	SAEC	small airway:	n/a
3	chr3:75448983-75449033	SKMC	muscle:	n/a
4	chr3:75411038-75411088	PFSK-1	brain:	n/a
5	chr3:75411217-75411267	Jurkat	blood:	n/a
6	chr3:75484516-75484566	SAEC	small airway:	n/a
7	chr3:75448983-75449033	SKMC	muscle:	n/a
8	chr3:75411038-75411088	PFSK-1	brain:	n/a
9	chr3:75412866-75412916	T-47D	breast:	n/a
10	chr3:75555938-75555988	ProgFib	skin:	n/a
11	chr3:75416171-75416221	HAEpiC	amniotic membrane:	n/a
12	chr3:75412866-75412916	Hepatocyte	liver:	n/a
13	chr3:75443047-75443097	AG04450	lung:	fetal
14	chr3:75481281-75481331	GM12878	blood:	n/a
15	chr3:75553762-75553812	SKMC	muscle:	n/a
16	chr3:75444752-75444802	HCPEpiC	choroid plexus:	n/a
17	chr3:75482182-75482232	AG10803	skin:	n/a
18	chr3:75445738-75445788	HEK293	kidney:	embryo
19	chr3:75412866-75412916	HEEpiC	esophagus:	n/a
20	chr3:75553723-75553773	MCF10A-Er-Src	breast:	n/a
21	chr3:75553762-75553812	GM06990	blood:	n/a
22	chr3:75413083-75413133	GM12891	blood:	n/a
23	chr3:75481281-75481331	SK-N-SH_RA	brain:	n/a
24	chr3:75482182-75482232	MCF10A-Er-Src	breast:	n/a
25	chr3:75445610-75445660	NB4	blood:	n/a
26	chr3:75413083-75413133	AG04450	lung:	fetal
27	chr3:75410789-75410839	GM12878	blood:	n/a
28	chr3:75553762-75553812	AG10803	skin:	n/a
29	chr3:75485110-75485160	U87	brain:	n/a
30	chr3:75553762-75553812	Hepatocyte	liver:	n/a
31	chr3:75553723-75553773	SK-N-SH_RA	brain:	n/a
32	chr3:75411217-75411267	HCPEpiC	choroid plexus:	n/a
33	chr3:75415561-75415611	HRCEpiC	kidney:	n/a
34	chr3:75415526-75415576	NB4	blood:	n/a
35	chr3:75411217-75411267	HIPEpiC	eye:	n/a
36	chr3:75445738-75445788	Jurkat	blood:	n/a
37	chr3:75483803-75483853	GM12878	blood:	n/a
38	chr3:75556027-75556077	BJ	skin:	n/a
39	chr3:75556027-75556077	AG09309	skin:	n/a
40	chr3:75481281-75481331	LNCaP	prostate:	n/a
41	chr3:75412866-75412916	HUVEC	blood vessel:	n/a
42	chr3:75445095-75445145	SK-N-SH	brain:	n/a
43	chr3:75484440-75484490	GM06990	blood:	n/a
44	chr3:75485448-75485498	MCF10A-Er-Src	breast:	n/a
45	chr3:75553723-75553773	HEK293	kidney:	embryo
46	chr3:75448983-75449033	AoSMC	blood vessel:	n/a
47	chr3:75414693-75414743	GM19239	blood:	n/a
48	chr3:75445502-75445552	HMEC	breast:	n/a
49	chr3:75487529-75487579	U87	brain:	n/a
50	chr3:75483803-75483853	AG04449	skin:	fetal

(count:7 , 50 per page) page: 1

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

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG2C-3	chr3:75484499-75484564	ENSG00000272690.1
2	lnc-FRG2C-3	chr3:75496316-75496447	ENSG00000272690.1
3	lnc-FRG2C-3	chr3:75501348-75501809	ENSG00000272690.1
4	lnc-FRG2C-3	chr3:75497520-75500553	NONHSAT090533
5	lnc-FRG2C-3	chr3:75485367-75485503	XLOC_002710
6	lnc-FRG2C-3	chr3:75500361-75500553	ENSG00000272690.1
7	lnc-FRG2C-3	chr3:75501683-75501802	ENSG00000272690.1
8	lnc-FRG2C-3	chr3:75486207-75486426	XLOC_002710
9	lnc-FRG2C-3	chr3:75501683-75501794	NONHSAT090533
10	lnc-FRG2C-3	chr3:75485928-75486426	XLOC_002710
11	lnc-FRG2C-3	chr3:75488905-75488988	XLOC_002710
12	lnc-FRG2C-3	chr3:75488905-75488997	XLOC_002710
13	lnc-FRG2C-3	chr3:75492659-75492775	XLOC_002710
14	lnc-FRG2C-3	chr3:75505768-75506637	ENSG00000272690.1
15	lnc-FRG2C-11	chr3:75570954-75571163	NONHSAT090534
16	lnc-FRG2C-3	chr3:75500361-75500553	ENSG00000272690.1
17	lnc-FRG2C-3	chr3:75492659-75492797	ENSG00000272690.1

No data

Variant related genes	Relation type
FAM86DP	TF binding region
ENSG00000266685	TF binding region
ENSG00000242953	TF binding region
OR7E55P	TF binding region
ENSG00000243794	TF binding region
OR7E22P	TF binding region
LSP1P2	TF binding region
ENPP7P2	TF binding region
ALG1L6P	TF binding region
ENSG00000272690	TF binding region
ENSG00000244699	TF binding region
FAM86DP	CpG island
ENSG00000266685	CpG island
ENSG00000242953	CpG island
OR7E55P	CpG island
ENSG00000243794	CpG island
OR7E22P	CpG island
LSP1P2	CpG island
ENPP7P2	CpG island
ALG1L6P	CpG island
ENSG00000272690	CpG island
ENSG00000244699	CpG island
ENSG00000168298	chromatin interactions
ENSG00000251287	chromatin interactions
ENSG00000158483	chromatin interactions
ENSG00000248243	chromatin interactions
ITGB1	miRNA target sites
SFRS5	miRNA target sites

Extended variants
information (count: 9027 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:9027 , 50 per page) page: 1 2 3 4 5 6 7 ... 181

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533031765	chr3:75407667-75407668	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs547510494	chr3:75407676-75407677	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs72499095	chr3:75407742-75407743	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs186402944	chr3:75407767-75407768	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs143774568	chr3:75407774-75407775	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs569952951	chr3:75407776-75407777	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs190033214	chr3:75407786-75407787	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs558747244	chr3:75407789-75407790	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs576965239	chr3:75407809-75407810	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs182355158	chr3:75407813-75407814	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs553859795	chr3:75407815-75407816	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs112858200	chr3:75407818-75407819	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs542635497	chr3:75407821-75407822	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs148100371	chr3:75407837-75407838	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs188290728	chr3:75407983-75407984	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs141895192	chr3:75408039-75408040	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs551914191	chr3:75408044-75408045	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs565519185	chr3:75408050-75408051	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs532741696	chr3:75408064-75408065	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs116596823	chr3:75408070-75408071	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs144987525	chr3:75408079-75408080	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs529782918	chr3:75408087-75408088	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs368104449	chr3:75408091-75408092	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs548181686	chr3:75408094-75408095	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs77452743	chr3:75408137-75408138	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs138829912	chr3:75408139-75408140	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs191031688	chr3:75408144-75408145	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs558566769	chr3:75408153-75408154	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs570375500	chr3:75408154-75408155	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs142649623	chr3:75408167-75408168	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs552722709	chr3:75408169-75408170	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs572222535	chr3:75408175-75408176	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs183752563	chr3:75408182-75408183	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs199620967	chr3:75408195-75408196	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs200446113	chr3:75408223-75408224	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs554976391	chr3:75408231-75408232	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs576441989	chr3:75408593-75408594	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs537050457	chr3:75408594-75408595	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs577824919	chr3:75408641-75408642	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs558962203	chr3:75408642-75408643	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs577625841	chr3:75408645-75408646	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs190938209	chr3:75410748-75410749	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs375158871	chr3:75410764-75410765	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs565994472	chr3:75410790-75410791	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs111856258	chr3:75410791-75410792	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs560687759	chr3:75410813-75410814	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs74830038	chr3:75410820-75410821	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs13076083	chr3:75410838-75410839	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs375829229	chr3:75411000-75411001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs571385389	chr3:75411006-75411007	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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

Chromatin state (count:1423 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75411000-75411400	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr3:75411000-75412000	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr3:75411000-75412200	Enhancers	Pancreas	Pancrea
4	chr3:75411000-75413400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr3:75411200-75411600	Enhancers	H1 Cell Line	embryonic stem cell
6	chr3:75411200-75411600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr3:75411600-75412400	Enhancers	Placenta	Placenta
8	chr3:75411600-75412800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr3:75411800-75412200	Enhancers	H1 Cell Line	embryonic stem cell
10	chr3:75412000-75413400	Enhancers	Stomach Mucosa	stomach
11	chr3:75413000-75413200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr3:75420200-75421800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr3:75421400-75423000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr3:75421800-75422600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr3:75422000-75422200	Flanking Active TSS	Osteobl	bone
16	chr3:75422000-75422400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr3:75422000-75422400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr3:75422000-75423000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr3:75422200-75422800	Enhancers	Osteobl	bone
20	chr3:75422600-75423000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr3:75423000-75423600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr3:75427600-75427800	Enhancers	Fetal Lung	lung
23	chr3:75427800-75428000	Enhancers	Fetal Heart	heart
24	chr3:75427800-75428200	Enhancers	Fetal Muscle Leg	muscle
25	chr3:75427800-75429000	Weak transcription	Fetal Lung	lung
26	chr3:75428000-75429000	Weak transcription	Fetal Heart	heart
27	chr3:75429000-75429200	Enhancers	Fetal Lung	lung
28	chr3:75429000-75429600	Enhancers	Fetal Heart	heart
29	chr3:75429000-75429600	Enhancers	Gastric	stomach
30	chr3:75429000-75429800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr3:75429000-75429800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr3:75429000-75429800	ZNF genes & repeats	Fetal Kidney	kidney
33	chr3:75429000-75429800	Enhancers	Pancreas	Pancrea
34	chr3:75429200-75429800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr3:75429200-75429800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr3:75429200-75429800	Active TSS	Fetal Lung	lung
37	chr3:75429200-75429800	ZNF genes & repeats	Dnd41	blood
38	chr3:75429400-75429800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr3:75429600-75429800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr3:75429800-75430200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr3:75429800-75445600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr3:75430000-75430200	Weak transcription	Fetal Kidney	kidney
43	chr3:75431600-75431800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr3:75431800-75432600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:75432000-75432200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr3:75432200-75433000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr3:75432600-75432800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr3:75432600-75433000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr3:75432800-75433400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr3:75435800-75436000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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