Variant report

Variant	nsv877148
Chromosome Location	chr3:88334311-88541582
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:451)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:451 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:88434387-88434629	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr3:88438892-88438979	K562	blood:	n/a	n/a
3	BACH1	chr3:88501523-88501717	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr3:88378808-88379094	IMR90	lung:	n/a	chr3:88378941-88378952
5	CEBPB	chr3:88528668-88528894	A549	lung:	n/a	n/a
6	CEBPB	chr3:88369030-88369230	A549	lung:	n/a	n/a
7	CEBPB	chr3:88396713-88396914	Hela-S3	cervix:	n/a	chr3:88396754-88396765
8	CEBPB	chr3:88528621-88528887	IMR90	lung:	n/a	n/a
9	CEBPB	chr3:88396623-88396919	HepG2	liver:	n/a	chr3:88396754-88396765
10	CEBPB	chr3:88515855-88516126	HepG2	liver:	n/a	chr3:88515996-88516007 chr3:88515997-88516006
11	CEBPB	chr3:88434165-88434583	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr3:88528652-88528747	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr3:88378823-88378968	HepG2	liver:	n/a	chr3:88378941-88378952
14	CEBPB	chr3:88370833-88371190	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr3:88396706-88396908	A549	lung:	n/a	chr3:88396754-88396765
16	CEBPB	chr3:88427165-88427365	H1-hESC	embryonic stem cell:	n/a	chr3:88427292-88427305
17	CHD1	chr3:88357026-88357066	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr3:88514040-88514190	HAc	cerebellar:	n/a	n/a
19	CTCF	chr3:88514020-88514170	HMEC	breast:	n/a	n/a
20	CTCF	chr3:88516440-88516590	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr3:88514000-88514150	Caco-2	colon:	n/a	n/a
22	CTCF	chr3:88366673-88366774	MCF-7	breast:	n/a	n/a
23	CTCF	chr3:88516420-88516570	Caco-2	colon:	n/a	n/a
24	CTCF	chr3:88519100-88519250	HAc	cerebellar:	n/a	n/a
25	CTCF	chr3:88516460-88516610	MCF-7	breast:	n/a	n/a
26	CTCF	chr3:88351660-88351810	GM12870	blood:	n/a	n/a
27	CTCF	chr3:88514078-88514170	MCF-7	breast:	n/a	n/a
28	CTCF	chr3:88514492-88514520	MCF-7	breast:	n/a	chr3:88514499-88514515
29	CTCF	chr3:88468481-88468493	GM13976	blood:	n/a	n/a
30	CTCF	chr3:88366675-88366780	MCF-7	breast:	n/a	n/a
31	CTCF	chr3:88514080-88514230	HMEC	breast:	n/a	n/a
32	CTCF	chr3:88383440-88383590	HCM	heart:	n/a	n/a
33	CTCF	chr3:88516460-88516610	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr3:88366691-88366812	HepG2	liver:	n/a	n/a
35	CTCF	chr3:88516500-88516650	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr3:88356440-88356590	AG09319	gingival:	n/a	n/a
37	CTCF	chr3:88366691-88366794	GM12892	blood:	n/a	n/a
38	CTCF	chr3:88516512-88516566	MCF-7	breast:	n/a	n/a
39	CTCF	chr3:88514020-88514170	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr3:88516500-88516650	HEK293	kidney:	n/a	n/a
41	CTCF	chr3:88366654-88366767	MCF-7	breast:	n/a	n/a
42	CTCF	chr3:88463612-88463648	GM20000	blood:	n/a	n/a
43	CTCF	chr3:88366668-88366851	MCF-7	breast:	n/a	n/a
44	CTCF	chr3:88516420-88516570	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr3:88514060-88514210	MCF-7	breast:	n/a	n/a
46	CTCF	chr3:88383460-88383610	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr3:88366680-88366797	MCF-7	breast:	n/a	n/a
48	CTCF	chr3:88449307-88449344	GM20000	blood:	n/a	n/a
49	CTCF	chr3:88514120-88514270	HRE	kidney:	n/a	n/a
50	CTCF	chr3:88514000-88514150	HBMEC	blood vessel:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:88352696-88352746	NB4	blood:	n/a
2	chr3:88352696-88352746	HIPEpiC	eye:	n/a
3	chr3:88352696-88352746	HRCEpiC	kidney:	n/a
4	chr3:88352696-88352746	MCF-7	breast:	n/a
5	chr3:88352696-88352746	NHBE	bronchial:	n/a
6	chr3:88352696-88352746	A549	lung:	n/a
7	chr3:88352696-88352746	U87	brain:	n/a
8	chr3:88352696-88352746	HepG2	liver:	n/a
9	chr3:88352696-88352746	HCM	heart:	n/a
10	chr3:88352696-88352746	HNPCEpiC	eye:	n/a
11	chr3:88352696-88352746	MCF10A-Er-Src	breast:	n/a
12	chr3:88352696-88352746	AG09319	gingival:	n/a
13	chr3:88352696-88352746	SAEC	small airway:	n/a
14	chr3:88352696-88352746	HRPEpiC	eye:	n/a
15	chr3:88352696-88352746	HMEC	breast:	n/a
16	chr3:88352696-88352746	SKMC	muscle:	n/a
17	chr3:88352696-88352746	CMK	blood:	n/a
18	chr3:88352696-88352746	T-47D	breast:	n/a
19	chr3:88352696-88352746	RPTEC	kidney:	n/a
20	chr3:88352696-88352746	AG09309	skin:	n/a
21	chr3:88352696-88352746	BE2_C	brain:	n/a
22	chr3:88352696-88352746	NHDF-neo	bronchial:	n/a
23	chr3:88352696-88352746	BJ	skin:	n/a
24	chr3:88352696-88352746	HCT-116	colon:	n/a
25	chr3:88352696-88352746	HEK293	kidney:	embryo
26	chr3:88352696-88352746	HAEpiC	amniotic membrane:	n/a
27	chr3:88352696-88352746	H1-hESC	embryonic stem cell:	embryo
28	chr3:88352696-88352746	AG04450	lung:	fetal
29	chr3:88352696-88352746	NT2-D1	testis:	n/a
30	chr3:88352696-88352746	HCPEpiC	choroid plexus:	n/a
31	chr3:88352696-88352746	LNCaP	prostate:	n/a
32	chr3:88352696-88352746	NH-A	brain:	n/a
33	chr3:88352696-88352746	PANC-1	pancreas:	n/a
34	chr3:88352696-88352746	SK-N-SH	brain:	n/a
35	chr3:88352696-88352746	SK-N-SH_RA	brain:	n/a
36	chr3:88352696-88352746	ProgFib	skin:	n/a
37	chr3:88352696-88352746	PrEC	prostate:	n/a
38	chr3:88352696-88352746	ovcar-3	ovarian:	n/a
39	chr3:88352696-88352746	GM12891	blood:	n/a
40	chr3:88352696-88352746	Jurkat	blood:	n/a
41	chr3:88352696-88352746	AG10803	skin:	n/a
42	chr3:88352696-88352746	GM06990	blood:	n/a
43	chr3:88352696-88352746	HUVEC	blood vessel:	n/a
44	chr3:88352696-88352746	Hepatocyte	liver:	n/a
45	chr3:88352696-88352746	GM19239	blood:	n/a
46	chr3:88352696-88352746	GM12892	blood:	n/a
47	chr3:88352696-88352746	HL-60	blood:	n/a
48	chr3:88352696-88352746	K562	blood:	n/a
49	chr3:88352696-88352746	Caco-2	colon:	n/a
50	chr3:88352696-88352746	PFSK-1	brain:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:88377277..88378950-chr3:88387834..88390220,2	MCF-7	breast:
2	chr3:88377277..88378950-chr3:88387834..88390220,2	MCF-7	breast:
3	chr3:88520234..88522396-chr3:88537772..88539509,2	K562	blood:
4	chr3:88443258..88445795-chr3:88448224..88450369,2	K562	blood:
5	chr20:7969749..7970528-chr3:88470088..88470821,2	MCF-7	breast:
6	chr3:88520234..88522396-chr3:88537772..88539509,2	K562	blood:
7	chr3:88526173..88527680-chr3:88528498..88531008,2	MCF-7	breast:
8	chr3:88356773..88358838-chr3:88359447..88361325,2	K562	blood:
9	chr3:88526173..88527680-chr3:88528498..88531008,2	MCF-7	breast:
10	chr3:88356773..88358838-chr3:88359447..88361325,2	K562	blood:
11	chr3:88348034..88350434-chr3:88355298..88358101,2	MCF-7	breast:
12	chr3:88348034..88350434-chr3:88355298..88358101,2	MCF-7	breast:
13	chr3:88443258..88445795-chr3:88448224..88450369,2	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C3orf38-2	chr3:88387591-88387793	XLOC_002727
2	lnc-C3orf38-2	chr3:88470263-88470483	l_2409_chr3:88470262-88514628_testes
3	lnc-C3orf38-2	chr3:88431735-88431938	XLOC_002727
4	lnc-C3orf38-2	chr3:88431734-88431938	NONHSAT090703
5	lnc-C3orf38-2	chr3:88387572-88387793	NONHSAT090703
6	lnc-C3orf38-2	chr3:88387573-88387793	XLOC_002727
7	lnc-C3orf38-2	chr3:88514238-88517304	XLOC_002727
8	lnc-C3orf38-2	chr3:88418571-88418634	XLOC_002727
9	lnc-C3orf38-2	chr3:88431735-88431938	XLOC_002727
10	lnc-C3orf38-2	chr3:88501234-88501324	l_2409_chr3:88470262-88514628_testes
11	lnc-C3orf38-2	chr3:88474992-88475125	l_2409_chr3:88470262-88514628_testes
12	lnc-C3orf38-2	chr3:88392302-88392435	XLOC_002727
13	lnc-C3orf38-2	chr3:88514425-88514628	l_2409_chr3:88470262-88514628_testes
14	lnc-C3orf38-2	chr3:88514238-88517156	XLOC_002727
15	lnc-C3orf38-2	chr3:88387573-88387793	XLOC_002727
16	lnc-C3orf38-2	chr3:88392301-88392435	NONHSAT090703

No data

Variant related genes	Relation type
ENSG00000207316	TF binding region
ABCF2P1	TF binding region
ENSG00000207316	CpG island
ABCF2P1	CpG island
BLCAP	miRNA target sites
ECE1	miRNA target sites
E2F8	miRNA target sites
VLDLR	miRNA target sites
HCCS	miRNA target sites

Extended variants
information (count: 2988 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2988 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6785442	chr3:88334311-88334312	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs140657630	chr3:88334382-88334383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554134310	chr3:88334393-88334394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs111651624	chr3:88334458-88334459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572621076	chr3:88334468-88334469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs66886233	chr3:88334478-88334479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs75304331	chr3:88334488-88334489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs56187053	chr3:88334489-88334490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs114027023	chr3:88334490-88334491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112401221	chr3:88334494-88334495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563848093	chr3:88334527-88334528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575203046	chr3:88334567-88334568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543093140	chr3:88334573-88334574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs56663975	chr3:88334585-88334586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528849926	chr3:88334647-88334648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188531878	chr3:88334711-88334712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371892362	chr3:88334725-88334726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533173268	chr3:88334726-88334727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551645085	chr3:88334845-88334846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192902688	chr3:88334927-88334928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538367244	chr3:88334938-88334939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564560187	chr3:88334940-88334941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs62269290	chr3:88334941-88334942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138691960	chr3:88334978-88334979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554450142	chr3:88335017-88335018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184269692	chr3:88335029-88335030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547113330	chr3:88335035-88335036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562128349	chr3:88335048-88335049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557958258	chr3:88335049-88335050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs142744949	chr3:88335077-88335078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543130289	chr3:88335096-88335097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs6788674	chr3:88335108-88335109	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs551267186	chr3:88335109-88335110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540630447	chr3:88335124-88335125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569585660	chr3:88335133-88335134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs79887094	chr3:88335151-88335152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs34386225	chr3:88335162-88335163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs114769964	chr3:88335188-88335189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533314037	chr3:88335189-88335190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs6777576	chr3:88335239-88335240	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs2061371	chr3:88335282-88335283	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs77659400	chr3:88335289-88335290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550268713	chr3:88335315-88335316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568414307	chr3:88335421-88335422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs139218891	chr3:88335428-88335429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547515296	chr3:88335450-88335451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs80111553	chr3:88335481-88335482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149407383	chr3:88335483-88335484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557995238	chr3:88335499-88335500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576252229	chr3:88335542-88335543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
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
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	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
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Soft tissue tumor	16732325	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
craniofacial dysmorphism	21918468	CNVD
Cancer	20164920	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22522925	CNVD
Lung cancer	19547694	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:131 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:88332400-88339800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr3:88333600-88334400	Enhancers	Small Intestine	intestine
3	chr3:88334200-88334400	Enhancers	Ovary	ovary
4	chr3:88339800-88342000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr3:88340400-88341200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr3:88340600-88341000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr3:88341200-88342000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr3:88347000-88347200	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr3:88347200-88347600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
10	chr3:88347200-88348000	Enhancers	Primary T cells from cord blood	blood
11	chr3:88347400-88347800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr3:88347600-88347800	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr3:88347800-88348000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
14	chr3:88347800-88350000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr3:88348000-88348600	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr3:88348600-88350000	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr3:88350000-88351000	Enhancers	Rectal Mucosa Donor 31	rectum
18	chr3:88350000-88352000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr3:88351000-88358600	Weak transcription	Right Atrium	heart
20	chr3:88352200-88352800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
21	chr3:88355200-88360000	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr3:88355400-88357400	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr3:88355600-88357000	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr3:88355600-88359000	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr3:88355600-88359800	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr3:88355800-88359400	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr3:88356000-88356200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr3:88356000-88356200	Enhancers	H1 Cell Line	embryonic stem cell
29	chr3:88356200-88356800	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr3:88356200-88358400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr3:88356800-88357000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr3:88356800-88357200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr3:88356800-88357200	Enhancers	Brain Germinal Matrix	brain
34	chr3:88356800-88357200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
35	chr3:88356800-88357200	Enhancers	Pancreas	Pancrea
36	chr3:88356800-88357600	Enhancers	H1 Cell Line	embryonic stem cell
37	chr3:88357000-88357200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr3:88357000-88357400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
39	chr3:88357000-88357800	Enhancers	H9 Cell Line	embryonic stem cell
40	chr3:88357400-88358000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr3:88357400-88358800	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr3:88358000-88359000	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr3:88358400-88359200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr3:88359000-88361000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr3:88360800-88362200	Enhancers	Fetal Lung	lung
46	chr3:88361000-88361200	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr3:88361000-88361800	Enhancers	Fetal Stomach	stomach
48	chr3:88365000-88366000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr3:88370400-88371200	Enhancers	Hela-S3	cervix
50	chr3:88370600-88370800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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