Variant report

Variant	nsv882751
Chromosome Location	chr5:116349590-116453954
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:442)
CpG islands
(count:305)
Chromatin interactive
region (count:17)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:442 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr5:116412789-116413197	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr5:116415297-116415412	GM12878	blood:	n/a	n/a
3	BHLHE40	chr5:116432856-116432901	GM12878	blood:	n/a	n/a
4	BHLHE40	chr5:116431280-116431297	GM12878	blood:	n/a	n/a
5	CCNT2	chr5:116361519-116361714	K562	blood:	n/a	n/a
6	CEBPB	chr5:116355462-116355747	A549	lung:	n/a	n/a
7	CEBPB	chr5:116439226-116439346	A549	lung:	n/a	chr5:116439273-116439284 chr5:116439271-116439284 chr5:116439273-116439284
8	CEBPB	chr5:116412765-116413339	HCT-116	colon:	n/a	n/a
9	CEBPB	chr5:116431280-116431588	HepG2	liver:	n/a	n/a
10	CEBPB	chr5:116408435-116408542	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr5:116355458-116355994	HepG2	liver:	n/a	n/a
12	CEBPB	chr5:116355475-116355742	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr5:116412844-116413184	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr5:116412840-116413211	MCF-7	breast:	n/a	n/a
15	CEBPB	chr5:116418691-116418876	HepG2	liver:	n/a	chr5:116418729-116418742
16	CHD2	chr5:116432777-116433017	GM12878	blood:	n/a	n/a
17	CHD2	chr5:116439421-116439555	GM12878	blood:	n/a	n/a
18	CTCF	chr5:116412980-116413130	AG04450	lung:	n/a	n/a
19	CTCF	chr5:116427683-116427771	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr5:116355499-116355594	LNCaP	prostate:	n/a	n/a
21	CTCF	chr5:116355440-116355590	MCF-7	breast:	n/a	n/a
22	CTCF	chr5:116412940-116413090	NB4	blood:	n/a	n/a
23	CTCF	chr5:116412902-116413110	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr5:116412940-116413090	HEK293	kidney:	n/a	n/a
25	CTCF	chr5:116412960-116413110	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr5:116413000-116413150	GM12870	blood:	n/a	n/a
27	CTCF	chr5:116412960-116413110	HPF	lung:	n/a	n/a
28	CTCF	chr5:116419920-116420070	RPTEC	kidney:	n/a	n/a
29	CTCF	chr5:116446401-116446525	MCF-7	breast:	n/a	n/a
30	CTCF	chr5:116419920-116420070	HEK293	kidney:	n/a	n/a
31	CTCF	chr5:116412960-116413110	HCM	heart:	n/a	n/a
32	CTCF	chr5:116412960-116413110	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr5:116412965-116413130	Pancreas_OC	pancreas:	n/a	n/a
34	CTCF	chr5:116412725-116413341	HCT-116	colon:	n/a	n/a
35	CTCF	chr5:116412940-116413090	GM12864	blood:	n/a	n/a
36	CTCF	chr5:116412980-116413130	HAc	cerebellar:	n/a	n/a
37	CTCF	chr5:116419880-116420030	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr5:116413300-116413394	GM20000	blood:	n/a	n/a
39	CTCF	chr5:116419857-116420012	NHEK	skin:	n/a	n/a
40	CTCF	chr5:116413000-116413150	HL-60	blood:	n/a	n/a
41	CTCF	chr5:116413000-116413150	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr5:116412940-116413090	GM12872	blood:	n/a	n/a
43	CTCF	chr5:116355490-116355602	MCF-7	breast:	n/a	n/a
44	CTCF	chr5:116412960-116413110	HA-sp	spinal cord:	n/a	n/a
45	CTCF	chr5:116419848-116419991	MCF-7	breast:	n/a	n/a
46	CTCF	chr5:116412920-116413070	GM12871	blood:	n/a	n/a
47	CTCF	chr5:116412940-116413090	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr5:116413000-116413150	BJ	skin:	n/a	n/a
49	CTCF	chr5:116419900-116420050	RPTEC	kidney:	n/a	n/a
50	CTCF	chr5:116412940-116413090	GM12878	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:116356275-116356325	AG04450	lung:	fetal
2	chr5:116385300-116385350	NHDF-neo	bronchial:	n/a
3	chr5:116355027-116355077	AG10803	skin:	n/a
4	chr5:116378307-116378357	AG10803	skin:	n/a
5	chr5:116385443-116385493	H1-hESC	embryonic stem cell:	embryo
6	chr5:116356275-116356325	HCF	heart:	n/a
7	chr5:116378307-116378357	AG09319	gingival:	n/a
8	chr5:116356275-116356325	NHDF-neo	bronchial:	n/a
9	chr5:116356275-116356325	GM12892	blood:	n/a
10	chr5:116355027-116355077	HIPEpiC	eye:	n/a
11	chr5:116355027-116355077	PrEC	prostate:	n/a
12	chr5:116385300-116385350	AG10803	skin:	n/a
13	chr5:116385443-116385493	Caco-2	colon:	n/a
14	chr5:116355027-116355077	BJ	skin:	n/a
15	chr5:116378307-116378357	HEEpiC	esophagus:	n/a
16	chr5:116385300-116385350	AoSMC	blood vessel:	n/a
17	chr5:116385443-116385493	RPTEC	kidney:	n/a
18	chr5:116385300-116385350	NB4	blood:	n/a
19	chr5:116356275-116356325	ECC-1	luminal epithelium:	n/a
20	chr5:116356275-116356325	RPTEC	kidney:	n/a
21	chr5:116385443-116385493	HCT-116	colon:	n/a
22	chr5:116355027-116355077	Jurkat	blood:	n/a
23	chr5:116385300-116385350	HRE	kidney:	n/a
24	chr5:116356275-116356325	NT2-D1	testis:	n/a
25	chr5:116385300-116385350	BJ	skin:	n/a
26	chr5:116356275-116356325	IMR90	lung:	fetal
27	chr5:116385300-116385350	H1-hESC	embryonic stem cell:	embryo
28	chr5:116385300-116385350	PFSK-1	brain:	n/a
29	chr5:116356275-116356325	PANC-1	pancreas:	n/a
30	chr5:116385443-116385493	NH-A	brain:	n/a
31	chr5:116385300-116385350	AG09319	gingival:	n/a
32	chr5:116385443-116385493	AG09319	gingival:	n/a
33	chr5:116378307-116378357	HepG2	liver:	n/a
34	chr5:116356275-116356325	Hela-S3	cervix:	n/a
35	chr5:116378307-116378357	PrEC	prostate:	n/a
36	chr5:116355027-116355077	SKMC	muscle:	n/a
37	chr5:116385300-116385350	IMR90	lung:	fetal
38	chr5:116385300-116385350	HNPCEpiC	eye:	n/a
39	chr5:116385443-116385493	IMR90	lung:	fetal
40	chr5:116385443-116385493	AG09309	skin:	n/a
41	chr5:116378307-116378357	CMK	blood:	n/a
42	chr5:116356275-116356325	AoSMC	blood vessel:	n/a
43	chr5:116378307-116378357	GM12891	blood:	n/a
44	chr5:116385300-116385350	SK-N-SH_RA	brain:	n/a
45	chr5:116378307-116378357	AG04450	lung:	fetal
46	chr5:116355027-116355077	SAEC	small airway:	n/a
47	chr5:116385443-116385493	PFSK-1	brain:	n/a
48	chr5:116378307-116378357	HRCEpiC	kidney:	n/a
49	chr5:116385443-116385493	Hela-S3	cervix:	n/a
50	chr5:116378307-116378357	GM19239	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:116412161..116414057-chr5:116417995..116420455,2	MCF-7	breast:
2	chr5:116403228..116405101-chr5:116405267..116406890,2	K562	blood:
3	chr5:116415643..116418388-chr5:116422613..116424563,2	MCF-7	breast:
4	chr5:116388114..116390786-chr5:116391482..116393970,2	K562	blood:
5	chr5:116412161..116414057-chr5:116417995..116420455,2	MCF-7	breast:
6	chr5:116360894..116363806-chr5:116375344..116377265,2	MCF-7	breast:
7	chr5:116412565..116413464-chr5:116601306..116602202,3	MCF-7	breast:
8	chr5:116381480..116384331-chr5:116390056..116392321,2	K562	blood:
9	chr5:116415643..116418388-chr5:116422613..116424563,2	MCF-7	breast:
10	chr5:116381480..116384331-chr5:116390056..116392321,2	K562	blood:
11	chr20:49334975..49335937-chr5:116357755..116358651,2	MCF-7	breast:
12	chr5:116360894..116363806-chr5:116375344..116377265,2	MCF-7	breast:
13	chr5:116370263..116371870-chr5:116372681..116375033,2	K562	blood:
14	chr4:181060859..181061364-chr5:116353318..116353952,2	MCF-7	breast:
15	chr5:116403228..116405101-chr5:116405267..116406890,2	K562	blood:
16	chr5:116370263..116371870-chr5:116372681..116375033,2	K562	blood:
17	chr5:116388114..116390786-chr5:116391482..116393970,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COMMD10-4	chr5:116366896-116367126	XLOC_004521
2	lnc-SEMA6A-8	chr5:116387796-116387856	NONHSAT103384
3	lnc-COMMD10-4	chr5:116374077-116374265	XLOC_004521
4	lnc-SEMA6A-8	chr5:116382515-116382695	NONHSAT103384

No data

Variant related genes	Relation type
ENSG00000250650	TF binding region
ENSG00000250949	TF binding region
ENSG00000250650	CpG island
ENSG00000250949	CpG island
RBFOX2	miRNA target sites

Extended variants
information (count: 4163 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:4163 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1459091	chr5:116349590-116349591	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs113233333	chr5:116349625-116349626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534924833	chr5:116349636-116349637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs555125997	chr5:116349646-116349647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs568686681	chr5:116349651-116349652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs537743824	chr5:116349653-116349654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs185759132	chr5:116349656-116349657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190697621	chr5:116349688-116349689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs576835138	chr5:116349700-116349701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs79699383	chr5:116349738-116349739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553072138	chr5:116349794-116349795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572987155	chr5:116349809-116349810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553758489	chr5:116349882-116349883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs145819187	chr5:116349905-116349906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182030269	chr5:116349909-116349910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561135577	chr5:116349911-116349912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529985241	chr5:116349987-116349988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs543711861	chr5:116349990-116349991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368651661	chr5:116349999-116350000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368314183	chr5:116350030-116350031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186193733	chr5:116350074-116350075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532169733	chr5:116350107-116350108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139030638	chr5:116350143-116350144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565812010	chr5:116350154-116350155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528164943	chr5:116350168-116350169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs142701584	chr5:116350230-116350231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190764135	chr5:116350237-116350238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182812792	chr5:116350252-116350253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115570230	chr5:116350281-116350282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570780968	chr5:116350318-116350319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559069332	chr5:116350359-116350360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs34103908	chr5:116350384-116350385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369186539	chr5:116350424-116350425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78981494	chr5:116350445-116350446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185729973	chr5:116350493-116350494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542300468	chr5:116350494-116350495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371911529	chr5:116350507-116350508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564977947	chr5:116350630-116350631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs376181097	chr5:116350645-116350646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533526415	chr5:116350662-116350663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555539601	chr5:116350694-116350695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574581391	chr5:116350832-116350833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369163728	chr5:116350837-116350838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552021655	chr5:116350844-116350845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs543225362	chr5:116350848-116350849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371803815	chr5:116350870-116350871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563593596	chr5:116350881-116350882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146017376	chr5:116350884-116350885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190048750	chr5:116350886-116350887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs542708274	chr5:116350901-116350902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:116349000-116349600	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr5:116349000-116349600	Enhancers	H1 Cell Line	embryonic stem cell
3	chr5:116349000-116349600	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr5:116349200-116349600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr5:116349200-116349600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr5:116349200-116349600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:116349200-116349600	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr5:116349200-116349600	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr5:116349200-116349600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr5:116349200-116349600	Enhancers	Esophagus	oesophagus
11	chr5:116349200-116349800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr5:116349400-116349600	Enhancers	H9 Cell Line	embryonic stem cell
13	chr5:116349400-116352800	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr5:116349600-116351000	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr5:116349600-116352800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr5:116349600-116354000	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr5:116349600-116354000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr5:116349600-116355400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr5:116349600-116358200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr5:116351000-116351200	Enhancers	H9 Cell Line	embryonic stem cell
21	chr5:116352800-116354600	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr5:116352800-116356600	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr5:116354000-116354200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr5:116354000-116354400	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr5:116354000-116354400	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr5:116354000-116354400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr5:116354000-116354400	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr5:116354400-116355400	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr5:116354400-116355400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr5:116354400-116355600	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr5:116354600-116355000	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr5:116355000-116356200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr5:116355400-116355600	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr5:116355400-116355800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr5:116355400-116356200	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr5:116355600-116356400	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr5:116356600-116366800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr5:116358200-116358600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr5:116361600-116362400	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr5:116362600-116366600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
41	chr5:116365200-116365800	Enhancers	Fetal Lung	lung
42	chr5:116366800-116367200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
43	chr5:116367200-116376400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr5:116369200-116369400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr5:116370600-116376600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr5:116372000-116372800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
47	chr5:116372800-116388200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr5:116373600-116374400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr5:116374000-116374200	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr5:116374200-116377000	Weak transcription	HUES64 Cell Line	embryonic stem cell

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