Variant report

Variant	nsv4968
Chromosome Location	chr5:115635771-115714856
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:575)
CpG islands
(count:610)
Chromatin interactive
region (count:14)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:575 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:115705390-115705679	K562	blood:	n/a	n/a
2	ATF1	chr5:115694484-115694974	K562	blood:	n/a	n/a
3	ATF1	chr5:115707706-115707979	K562	blood:	n/a	n/a
4	ATF1	chr5:115679669-115679868	K562	blood:	n/a	n/a
5	ATF1	chr5:115700581-115701001	K562	blood:	n/a	n/a
6	ATF2	chr5:115700598-115701276	GM12878	blood:	n/a	n/a
7	ATF2	chr5:115694360-115694992	GM12878	blood:	n/a	n/a
8	ATF2	chr5:115697348-115697730	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr5:115694460-115695182	GM12878	blood:	n/a	n/a
10	BACH1	chr5:115697108-115697625	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr5:115679748-115679880	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr5:115700938-115701321	GM12878	blood:	n/a	n/a
13	BATF	chr5:115708897-115709253	GM12878	blood:	n/a	chr5:115709039-115709049 chr5:115709038-115709049
14	BATF	chr5:115700697-115701341	GM12878	blood:	n/a	chr5:115700750-115700759
15	BATF	chr5:115710093-115710344	GM12878	blood:	n/a	n/a
16	BATF	chr5:115694520-115694822	GM12878	blood:	n/a	n/a
17	BCL11A	chr5:115694461-115694921	GM12878	blood:	n/a	n/a
18	BCL11A	chr5:115700601-115701297	GM12878	blood:	n/a	n/a
19	BCL11A	chr5:115694504-115694827	GM12878	blood:	n/a	n/a
20	BCLAF1	chr5:115700651-115701235	GM12878	blood:	n/a	n/a
21	BHLHE40	chr5:115693915-115694099	K562	blood:	n/a	n/a
22	BHLHE40	chr5:115694534-115695030	GM12878	blood:	n/a	n/a
23	BRCA1	chr5:115697507-115697634	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr5:115697095-115697306	H1-hESC	embryonic stem cell:	n/a	n/a
25	CBX3	chr5:115644136-115644420	K562	blood:	n/a	n/a
26	CBX3	chr5:115644114-115644421	K562	blood:	n/a	n/a
27	CBX3	chr5:115700646-115700980	K562	blood:	n/a	n/a
28	CBX3	chr5:115644032-115644480	HCT-116	colon:	n/a	n/a
29	CCNT2	chr5:115697493-115697603	K562	blood:	n/a	n/a
30	CCNT2	chr5:115700630-115700894	K562	blood:	n/a	n/a
31	CCNT2	chr5:115694584-115694957	K562	blood:	n/a	n/a
32	CCNT2	chr5:115705739-115705939	K562	blood:	n/a	n/a
33	CEBPB	chr5:115675270-115675603	A549	lung:	n/a	chr5:115675428-115675439
34	CEBPB	chr5:115635639-115636210	MCF-7	breast:	n/a	chr5:115635913-115635925
35	CEBPB	chr5:115675261-115675615	HepG2	liver:	n/a	chr5:115675428-115675439
36	CEBPB	chr5:115703591-115703827	IMR90	lung:	n/a	n/a
37	CEBPB	chr5:115707670-115707993	K562	blood:	n/a	n/a
38	CEBPB	chr5:115658862-115658938	A549	lung:	n/a	chr5:115658862-115658873
39	CEBPB	chr5:115675292-115675592	IMR90	lung:	n/a	chr5:115675428-115675439
40	CEBPB	chr5:115675360-115675580	Hela-S3	cervix:	n/a	chr5:115675428-115675439
41	CEBPB	chr5:115691836-115692123	HepG2	liver:	n/a	n/a
42	CEBPB	chr5:115707662-115708000	HepG2	liver:	n/a	n/a
43	CEBPB	chr5:115658782-115659034	HepG2	liver:	n/a	chr5:115658862-115658873
44	CEBPB	chr5:115682604-115682876	IMR90	lung:	n/a	n/a
45	CEBPB	chr5:115703505-115703776	K562	blood:	n/a	n/a
46	CEBPB	chr5:115707765-115707898	HepG2	liver:	n/a	n/a
47	CEBPB	chr5:115697104-115697566	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD1	chr5:115694640-115695218	GM12878	blood:	n/a	n/a
49	CHD1	chr5:115697074-115697311	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chr5:115696034-115696192	GM12878	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:115697696-115697746	ovcar-3	ovarian:	n/a
2	chr5:115693708-115693758	HPAEpiC	pulmonary alveolar:	n/a
3	chr5:115712252-115712302	AG09319	gingival:	n/a
4	chr5:115697696-115697746	SK-N-SH	brain:	n/a
5	chr5:115639617-115639667	GM12891	blood:	n/a
6	chr5:115712252-115712302	HRPEpiC	eye:	n/a
7	chr5:115696151-115696201	HRPEpiC	eye:	n/a
8	chr5:115697370-115697420	Caco-2	colon:	n/a
9	chr5:115693708-115693758	NT2-D1	testis:	n/a
10	chr5:115697446-115697496	HCPEpiC	choroid plexus:	n/a
11	chr5:115712252-115712302	Jurkat	blood:	n/a
12	chr5:115697588-115697638	HUVEC	blood vessel:	n/a
13	chr5:115712252-115712302	GM12892	blood:	n/a
14	chr5:115697446-115697496	H1-hESC	embryonic stem cell:	embryo
15	chr5:115697214-115697264	HCM	heart:	n/a
16	chr5:115697370-115697420	AG09309	skin:	n/a
17	chr5:115712252-115712302	SK-N-SH	brain:	n/a
18	chr5:115697214-115697264	HNPCEpiC	eye:	n/a
19	chr5:115696151-115696201	SAEC	small airway:	n/a
20	chr5:115697370-115697420	NT2-D1	testis:	n/a
21	chr5:115697214-115697264	HMEC	breast:	n/a
22	chr5:115696151-115696201	T-47D	breast:	n/a
23	chr5:115693708-115693758	RPTEC	kidney:	n/a
24	chr5:115712252-115712302	NHDF-neo	bronchial:	n/a
25	chr5:115697588-115697638	HPAEpiC	pulmonary alveolar:	n/a
26	chr5:115697446-115697496	GM06990	blood:	n/a
27	chr5:115697696-115697746	A549	lung:	n/a
28	chr5:115697446-115697496	HepG2	liver:	n/a
29	chr5:115697214-115697264	HL-60	blood:	n/a
30	chr5:115697446-115697496	AG10803	skin:	n/a
31	chr5:115696151-115696201	NHDF-neo	bronchial:	n/a
32	chr5:115697588-115697638	AG09319	gingival:	n/a
33	chr5:115697214-115697264	MCF-7	breast:	n/a
34	chr5:115697214-115697264	H1-hESC	embryonic stem cell:	embryo
35	chr5:115697370-115697420	HEEpiC	esophagus:	n/a
36	chr5:115696151-115696201	SKMC	muscle:	n/a
37	chr5:115693708-115693758	U87	brain:	n/a
38	chr5:115697696-115697746	HIPEpiC	eye:	n/a
39	chr5:115697370-115697420	HCT-116	colon:	n/a
40	chr5:115712252-115712302	GM12878	blood:	n/a
41	chr5:115712252-115712302	BJ	skin:	n/a
42	chr5:115697370-115697420	NHBE	bronchial:	n/a
43	chr5:115639617-115639667	LNCaP	prostate:	n/a
44	chr5:115696151-115696201	GM12891	blood:	n/a
45	chr5:115697214-115697264	AoSMC	blood vessel:	n/a
46	chr5:115697370-115697420	Hela-S3	cervix:	n/a
47	chr5:115693708-115693758	HCPEpiC	choroid plexus:	n/a
48	chr5:115693708-115693758	GM06990	blood:	n/a
49	chr5:115697588-115697638	HAEpiC	amniotic membrane:	n/a
50	chr5:115697370-115697420	HIPEpiC	eye:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:115693595..115697814-chr5:115698835..115703078,5	K562	blood:
2	chr5:115693595..115697814-chr5:115698835..115703078,5	K562	blood:
3	chr5:115647669..115649812-chr5:115683571..115685304,2	K562	blood:
4	chr5:115704428..115706706-chr5:115709540..115711421,2	MCF-7	breast:
5	chr5:115704428..115706706-chr5:115709540..115711421,2	MCF-7	breast:
6	chr5:115632385..115634405-chr5:115635053..115637473,2	K562	blood:
7	chr5:115714143..115716016-chr5:115739014..115740918,2	K562	blood:
8	chr5:115711711..115714418-chr5:115718644..115720507,2	K562	blood:
9	chr5:115647669..115649812-chr5:115683571..115685304,2	K562	blood:
10	chr5:115685651..115688638-chr5:115690874..115693480,2	K562	blood:
11	chr5:115630950..115633524-chr5:115633964..115636710,2	MCF-7	breast:
12	chr5:115692236..115694986-chr5:115697167..115699493,2	MCF-7	breast:
13	chr5:115692236..115694986-chr5:115697167..115699493,2	MCF-7	breast:
14	chr5:115685651..115688638-chr5:115690874..115693480,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COMMD10-6	chr5:115661716-115661988	l_3000_chr5:115661715-115668338_thyroid
2	lnc-LVRN.1-4	chr5:115639227-115639380	NONHSAT103358
3	lnc-LVRN.1-4	chr5:115638966-115639380	NONHSAT103359
4	lnc-COMMD10-6	chr5:115667915-115668338	l_3000_chr5:115661715-115668338_thyroid
5	lnc-SEMA6A-1	chr5:115708676-115708786	ENSG00000249280
6	lnc-SEMA6A-1	chr5:115708676-115708786	NONHSAT103361
7	lnc-SEMA6A-1	chr5:115703287-115706170	ENSG00000249280
8	lnc-LVRN.1-4	chr5:115641553-115642622	NONHSAT103359
9	lnc-SEMA6A-1	chr5:115710179-115710267	ENSG00000249280
10	lnc-SEMA6A-1	chr5:115710179-115710267	NONHSAT103361
11	lnc-SEMA6A-1	chr5:115703113-115706170	NONHSAT103361
12	lnc-COMMD10-6	chr5:115667126-115667860	l_3000_chr5:115661715-115668338_thyroid
13	lnc-LVRN.1-4	chr5:115643332-115643482	NONHSAT103359
14	lnc-LVRN.1-4	chr5:115637354-115638100	NONHSAT103359

No data

Variant related genes	Relation type
ENSG00000250015	TF binding region
ENSG00000250015	CpG island
ACACA	miRNA target sites
BBC3	miRNA target sites
USP15	miRNA target sites

Extended variants
information (count: 3784 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:3784 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558848812	chr5:115635774-115635775	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs153594	chr5:115635788-115635789	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs149169821	chr5:115635793-115635794	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs144961984	chr5:115635819-115635820	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188447860	chr5:115635893-115635894	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs153593	chr5:115635903-115635904	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs58424191	chr5:115635935-115635936	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs564028466	chr5:115635963-115635964	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577454909	chr5:115635966-115635967	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs546408263	chr5:115635993-115635994	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs138829339	chr5:115636030-115636031	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs10463683	chr5:115636031-115636032	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs114562308	chr5:115636064-115636065	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs560919971	chr5:115636117-115636118	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs58791417	chr5:115636164-115636165	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549477737	chr5:115636195-115636196	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs551147440	chr5:115636198-115636199	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142232315	chr5:115636200-115636201	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538534119	chr5:115636216-115636217	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs35745074	chr5:115636258-115636259	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552395445	chr5:115636279-115636280	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs34360216	chr5:115636289-115636290	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541804955	chr5:115636295-115636296	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs192531067	chr5:115636301-115636302	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs375789033	chr5:115636342-115636343	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs111998609	chr5:115636343-115636344	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs200935783	chr5:115636344-115636345	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs35424111	chr5:115636364-115636365	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534466821	chr5:115636379-115636380	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs554643948	chr5:115636390-115636391	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139162085	chr5:115636406-115636407	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs146406104	chr5:115636421-115636422	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs574562801	chr5:115636457-115636458	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs148139581	chr5:115636486-115636487	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs557059255	chr5:115636514-115636515	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577514822	chr5:115636573-115636574	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs17139435	chr5:115636597-115636598	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs559959134	chr5:115636612-115636613	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573478896	chr5:115636629-115636630	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542413803	chr5:115636702-115636703	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs117880774	chr5:115636728-115636729	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529687587	chr5:115636808-115636809	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529799250	chr5:115636812-115636813	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs571076199	chr5:115636840-115636841	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs549775154	chr5:115636852-115636853	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs185351741	chr5:115636891-115636892	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs532477317	chr5:115636908-115636909	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552197568	chr5:115636918-115636919	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188267842	chr5:115636935-115636936	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs192074611	chr5:115636947-115636948	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Sezary syndrome	18413736	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1631 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:115613400-115641600	Weak transcription	HSMM	muscle
2	chr5:115625600-115639200	Weak transcription	Fetal Stomach	stomach
3	chr5:115625600-115643000	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr5:115626600-115641600	Weak transcription	Fetal Brain Male	brain
5	chr5:115626800-115642200	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr5:115627800-115639200	Weak transcription	Placenta	Placenta
7	chr5:115628000-115643800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr5:115628400-115639200	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr5:115628400-115641200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr5:115628600-115639400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr5:115628600-115643400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr5:115629000-115643800	Weak transcription	HUVEC	blood vessel
13	chr5:115629400-115638200	Weak transcription	Pancreas	Pancrea
14	chr5:115629400-115638400	Weak transcription	Right Ventricle	heart
15	chr5:115631400-115636200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr5:115631400-115637800	Weak transcription	Fetal Thymus	thymus
17	chr5:115631800-115640600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr5:115631800-115641800	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr5:115632000-115639200	Weak transcription	Lung	lung
20	chr5:115632000-115643000	Weak transcription	NH-A	brain
21	chr5:115632600-115640400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr5:115632600-115640600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr5:115632600-115643400	Weak transcription	Stomach Mucosa	stomach
24	chr5:115632800-115639600	Weak transcription	Brain Angular Gyrus	brain
25	chr5:115632800-115642600	Weak transcription	NHDF-Ad	bronchial
26	chr5:115633000-115635800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr5:115633200-115640800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr5:115633600-115639800	Weak transcription	Spleen	Spleen
29	chr5:115633800-115637600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr5:115633800-115638200	Weak transcription	HSMMtube	muscle
31	chr5:115633800-115640400	Weak transcription	Esophagus	oesophagus
32	chr5:115634000-115637800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr5:115634000-115640400	Strong transcription	Primary monocytes fromperipheralblood	blood
34	chr5:115634200-115636000	Weak transcription	Fetal Lung	lung
35	chr5:115634200-115636800	Strong transcription	Primary T helper cells PMA-I stimulated	--
36	chr5:115634200-115637400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr5:115634200-115637600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr5:115634200-115637600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr5:115634200-115639000	Weak transcription	Small Intestine	intestine
40	chr5:115634200-115639200	Weak transcription	Cortex derived primary cultured neurospheres	brain
41	chr5:115634200-115639200	Weak transcription	Colonic Mucosa	Colon
42	chr5:115634200-115639200	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr5:115634200-115639400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr5:115634200-115639400	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr5:115634200-115639600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr5:115634200-115639600	Weak transcription	Dnd41	blood
47	chr5:115634200-115640200	Weak transcription	Stomach Smooth Muscle	stomach
48	chr5:115634200-115640400	Weak transcription	Fetal Intestine Small	intestine
49	chr5:115634200-115640600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr5:115634200-115640600	Weak transcription	Thymus	Thymus

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