Variant report

Variant	esv3490712
Chromosome Location	chr5:69311497-70160360
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:9601)
CpG islands
(count:549)
Chromatin interactive
region (count:0)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:9601 , 50 per page) page: 1 2 3 4 5 6 7 ... 193

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:69696778-69696970	K562	blood:	n/a	n/a
2	ATF3	chr5:69696877-69696999	K562	blood:	n/a	n/a
3	BATF	chr5:69602112-69602362	GM12878	blood:	n/a	n/a
4	BATF	chr5:70058347-70059128	GM12878	blood:	n/a	n/a
5	BATF	chr5:69854534-69854815	GM12878	blood:	n/a	chr5:69854638-69854647
6	BATF	chr5:69585509-69586062	GM12878	blood:	n/a	n/a
7	BATF	chr5:69894017-69894214	GM12878	blood:	n/a	n/a
8	BATF	chr5:70043640-70043922	GM12878	blood:	n/a	n/a
9	BATF	chr5:69539188-69539612	GM12878	blood:	n/a	n/a
10	BATF	chr5:69897698-69897890	GM12878	blood:	n/a	n/a
11	BATF	chr5:70002912-70003149	GM12878	blood:	n/a	n/a
12	BATF	chr5:69881708-69882291	GM12878	blood:	n/a	n/a
13	BATF	chr5:70043256-70043537	GM12878	blood:	n/a	chr5:70043459-70043468
14	BATF	chr5:69886310-69886585	GM12878	blood:	n/a	chr5:69886491-69886501
15	BATF	chr5:69405258-69405604	GM12878	blood:	n/a	n/a
16	BATF	chr5:69696601-69696886	GM12878	blood:	n/a	n/a
17	BATF	chr5:70015590-70016239	GM12878	blood:	n/a	n/a
18	BATF	chr5:69573125-69573369	GM12878	blood:	n/a	n/a
19	BATF	chr5:69684520-69684757	GM12878	blood:	n/a	n/a
20	BATF	chr5:69541303-69542084	GM12878	blood:	n/a	n/a
21	BATF	chr5:69584879-69585193	GM12878	blood:	n/a	n/a
22	BATF	chr5:70060822-70061246	GM12878	blood:	n/a	n/a
23	BATF	chr5:69598427-69598711	GM12878	blood:	n/a	n/a
24	BATF	chr5:69710854-69711383	GM12878	blood:	n/a	n/a
25	BATF	chr5:69617477-69617689	GM12878	blood:	n/a	n/a
26	BATF	chr5:69878333-69878563	GM12878	blood:	n/a	n/a
27	BATF	chr5:69701063-69701468	GM12878	blood:	n/a	n/a
28	BATF	chr5:69920978-69921204	GM12878	blood:	n/a	n/a
29	BATF	chr5:69554897-69555110	GM12878	blood:	n/a	n/a
30	BATF	chr5:70111545-70111758	GM12878	blood:	n/a	n/a
31	BATF	chr5:70028362-70028636	GM12878	blood:	n/a	n/a
32	BATF	chr5:69580804-69581247	GM12878	blood:	n/a	n/a
33	BATF	chr5:69696587-69697198	GM12878	blood:	n/a	n/a
34	BATF	chr5:69538324-69538723	GM12878	blood:	n/a	n/a
35	BATF	chr5:69702143-69702413	GM12878	blood:	n/a	n/a
36	BATF	chr5:69584909-69585222	GM12878	blood:	n/a	n/a
37	BATF	chr5:69882386-69883123	GM12878	blood:	n/a	n/a
38	BATF	chr5:69695546-69695921	GM12878	blood:	n/a	n/a
39	BATF	chr5:70018767-70018986	GM12878	blood:	n/a	n/a
40	BATF	chr5:70019070-70019445	GM12878	blood:	n/a	n/a
41	BATF	chr5:69601166-69601370	GM12878	blood:	n/a	n/a
42	BATF	chr5:69835564-69835988	GM12878	blood:	n/a	n/a
43	BATF	chr5:69695755-69696492	GM12878	blood:	n/a	n/a
44	BATF	chr5:69473052-69473265	GM12878	blood:	n/a	n/a
45	BATF	chr5:70022457-70022912	GM12878	blood:	n/a	n/a
46	BATF	chr5:69991355-69991558	GM12878	blood:	n/a	n/a
47	BATF	chr5:69999361-69999611	GM12878	blood:	n/a	chr5:69999369-69999378
48	BATF	chr5:70058356-70059133	GM12878	blood:	n/a	n/a
49	BATF	chr5:70027009-70027232	GM12878	blood:	n/a	n/a
50	BATF	chr5:69704209-69704514	GM12878	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:69371421-69371471	HEK293	kidney:	embryo
2	chr5:69784092-69784142	HepG2	liver:	n/a
3	chr5:69483768-69483818	NH-A	brain:	n/a
4	chr5:69371421-69371471	AG10803	skin:	n/a
5	chr5:69784092-69784142	SK-N-SH_RA	brain:	n/a
6	chr5:69804518-69804568	Caco-2	colon:	n/a
7	chr5:69483768-69483818	H1-hESC	embryonic stem cell:	embryo
8	chr5:69483768-69483818	HEEpiC	esophagus:	n/a
9	chr5:69783979-69784029	HUVEC	blood vessel:	n/a
10	chr5:69371421-69371471	HIPEpiC	eye:	n/a
11	chr5:69804518-69804568	HRE	kidney:	n/a
12	chr5:69345099-69345149	GM12878	blood:	n/a
13	chr5:69345099-69345149	SK-N-SH	brain:	n/a
14	chr5:69697369-69697419	HIPEpiC	eye:	n/a
15	chr5:69804518-69804568	T-47D	breast:	n/a
16	chr5:69804518-69804568	GM12891	blood:	n/a
17	chr5:69803286-69803336	HNPCEpiC	eye:	n/a
18	chr5:69345099-69345149	HMEC	breast:	n/a
19	chr5:69783979-69784029	Hepatocyte	liver:	n/a
20	chr5:69325031-69325081	U87	brain:	n/a
21	chr5:69784092-69784142	A549	lung:	n/a
22	chr5:69345099-69345149	PFSK-1	brain:	n/a
23	chr5:69325031-69325081	AoSMC	blood vessel:	n/a
24	chr5:69345099-69345149	HAEpiC	amniotic membrane:	n/a
25	chr5:69784092-69784142	MCF10A-Er-Src	breast:	n/a
26	chr5:69784092-69784142	AG09319	gingival:	n/a
27	chr5:69345099-69345149	HIPEpiC	eye:	n/a
28	chr5:69803286-69803336	RPTEC	kidney:	n/a
29	chr5:69345099-69345149	U87	brain:	n/a
30	chr5:69483768-69483818	CMK	blood:	n/a
31	chr5:69784092-69784142	GM12891	blood:	n/a
32	chr5:69345099-69345149	GM12892	blood:	n/a
33	chr5:69804518-69804568	NT2-D1	testis:	n/a
34	chr5:69483768-69483818	HCT-116	colon:	n/a
35	chr5:69345099-69345149	K562	blood:	n/a
36	chr5:69697369-69697419	GM06990	blood:	n/a
37	chr5:69783979-69784029	SK-N-SH_RA	brain:	n/a
38	chr5:69371421-69371471	GM06990	blood:	n/a
39	chr5:69804518-69804568	SAEC	small airway:	n/a
40	chr5:69325031-69325081	PFSK-1	brain:	n/a
41	chr5:69371421-69371471	ProgFib	skin:	n/a
42	chr5:69804518-69804568	MCF10A-Er-Src	breast:	n/a
43	chr5:69803286-69803336	HIPEpiC	eye:	n/a
44	chr5:69483768-69483818	Hela-S3	cervix:	n/a
45	chr5:69784092-69784142	HL-60	blood:	n/a
46	chr5:69371421-69371471	ECC-1	luminal epithelium:	n/a
47	chr5:69345099-69345149	ProgFib	skin:	n/a
48	chr5:69803286-69803336	SK-N-MC	brain:	n/a
49	chr5:69371421-69371471	HL-60	blood:	n/a
50	chr5:69371421-69371471	NHDF-neo	bronchial:	n/a

No data

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SERF1A-2	chr5:70146637-70146751	NONHSAT101987
2	lnc-SERF1A-2	chr5:70149363-70149508	NONHSAT101987
3	lnc-NAIP-3	chr5:69733322-69734405	NONHSAT101975
4	lnc-NAIP-5	chr5:69435402-69435547	NONHSAT101964
5	lnc-SMN2-1	chr5:69321821-69321880	NONHSAT101949
6	lnc-NAIP-5	chr5:69438158-69438272	NONHSAT101964
7	lnc-SMN2-1	chr5:69322234-69322342	NONHSAT101949
8	lnc-SMN2-2	chr5:69745463-69746180	ENSG00000269983.1
9	lnc-SERF1B-2	chr5:69372740-69373356	NONHSAT101960
10	lnc-SERF1B-3	chr5:69370673-69370944	NONHSAT101959
11	lnc-SMN2-1	chr5:69321390-69321558	NONHSAT101949
12	lnc-TAF9-8	chr5:69351645-69353243	NONHSAT101952
13	lnc-SERF1A-2	chr5:70091602-70091743	NONHSAT101987
14	lnc-NAIP-5	chr5:69493082-69493223	NONHSAT101964
15	lnc-NAIP-2	chr5:69776697-69777165	NONHSAT101978

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SMN2	hsa-miR-30a-5p	chr5:69373364-69373385
2	SMN2	hsa-miR-186-5p	chr5:69373391-69373414
3	SMN2	hsa-miR-132-3p	chr5:69373197-69373218

Variant related genes	Relation type
ENSG00000251007	TF binding region
ENSG00000253333	TF binding region
ENSG00000250867	TF binding region
ENSG00000253816	TF binding region
CDH12P1	TF binding region
ENSG00000237075	TF binding region
CDH12P3	TF binding region
ENSG00000205565	TF binding region
ENSG00000253366	TF binding region
ENSG00000250918	TF binding region
SERF1B	TF binding region
ENSG00000196302	TF binding region
SMN2	TF binding region
ENSG00000197284	TF binding region
ENSG00000254701	TF binding region
RN7SL9P	TF binding region
ENSG00000250687	TF binding region
GTF2H2B	TF binding region
ENSG00000179978	TF binding region
ENSG00000269983	TF binding region
ENSG00000251007	CpG island
ENSG00000253333	CpG island
ENSG00000250867	CpG island
ENSG00000253816	CpG island
CDH12P1	CpG island
ENSG00000237075	CpG island
CDH12P3	CpG island
ENSG00000205565	CpG island
ENSG00000253366	CpG island
ENSG00000250918	CpG island
SERF1B	CpG island
ENSG00000196302	CpG island
SMN2	CpG island
ENSG00000197284	CpG island
ENSG00000254701	CpG island
RN7SL9P	CpG island
ENSG00000250687	CpG island
GTF2H2B	CpG island
ENSG00000179978	CpG island
ENSG00000269983	CpG island
GLCE	miRNA target sites

Extended variants
information (count: 937 )
Associated
traits (count: 127 )

Variant overlapped rSNPs/rCNVs (count:937 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62374798	chr5:69320757-69320758	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs200195287	chr5:69321892-69321893	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs79629075	chr5:69323596-69323597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113190250	chr5:69323700-69323701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555406718	chr5:69324248-69324249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573878951	chr5:69324269-69324270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs540883239	chr5:69324761-69324762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559133977	chr5:69324769-69324770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577385302	chr5:69324933-69324934	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs541213410	chr5:69324965-69324966	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs251156	chr5:69324995-69324996	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs544726860	chr5:69325043-69325044	Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs541713117	chr5:69325072-69325073	Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs530458632	chr5:69325076-69325077	Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs548954982	chr5:69325077-69325078	Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs560851875	chr5:69325083-69325084	Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs561472918	chr5:69325084-69325085	Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs528796235	chr5:69325097-69325098	Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs547273396	chr5:69325216-69325217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571883500	chr5:69325221-69325222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539205336	chr5:69325242-69325243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550821969	chr5:69325254-69325255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376798294	chr5:69325271-69325272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554508164	chr5:69325272-69325273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569316753	chr5:69325308-69325309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs529771991	chr5:69325463-69325464	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536298705	chr5:69325585-69325586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376700928	chr5:69325589-69325590	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572863105	chr5:69325924-69325925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534621475	chr5:69327460-69327461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549871808	chr5:69327577-69327578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552822020	chr5:69327935-69327936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577445158	chr5:69328024-69328025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545172694	chr5:69328148-69328149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78889138	chr5:69329788-69329789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563280804	chr5:69331175-69331176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376385953	chr5:69331192-69331193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201890206	chr5:69331212-69331213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2591359	chr5:69331213-69331214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs152885	chr5:69331216-69331217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372174012	chr5:69331219-69331220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542311013	chr5:69331496-69331497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560947144	chr5:69331499-69331500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200895078	chr5:69331509-69331510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs62374799	chr5:69332217-69332218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs62374800	chr5:69332250-69332251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs251141	chr5:69332256-69332257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528056944	chr5:69332414-69332415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547337478	chr5:69332420-69332421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201867570	chr5:69332452-69332453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:127)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ovarian cancer	21781307	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	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
Hepatocellular carcinoma	16750200	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
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
abnormal development	18461090	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21045282	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelodysplastic syndrome	18663149	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Sezary syndrome	18413736	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21990379	CNVD
Hirschsprung''s Disease	21712996	CNVD
Apoptosis	19488400	CNVD
Breast cancer	22048815	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Acute monocytic leukemia	16498392	CNVD
Colorectal cancer	20459617	CNVD
Gastric adenocarcinoma	19115996	CNVD
Spinal muscular atrophy	17160897	CNVD
Spinal muscular atrophy	17668391	CNVD
Spinal muscular atrophy	17668395	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pseudo-TORCH syndrome	20727516	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Obesity	21131291	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	21364760	CNVD
Mental retardation	20877625	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Spinal muscular atrophy	17647030	CNVD
Spinal muscular atrophy	20937953	CNVD
Spinal muscular atrophy	20442745	CNVD
Spinal muscular atrophy	21227393	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Disease	19212409	CNVD
Schizophrenia	21346763	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:382 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:69323200-69324800	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr5:69323200-69324800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr5:69323200-69325400	Weak transcription	Brain Anterior Caudate	brain
4	chr5:69323600-69345000	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr5:69323800-69326200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr5:69323800-69326600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr5:69324000-69326400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr5:69324800-69325000	Active TSS	Placenta	Placenta
9	chr5:69324800-69325200	Strong transcription	HUES48 Cell Line	embryonic stem cell
10	chr5:69324800-69325200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr5:69325000-69325200	Flanking Active TSS	Placenta	Placenta
12	chr5:69325200-69327800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr5:69325200-69344800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr5:69325400-69325800	Strong transcription	Brain Anterior Caudate	brain
15	chr5:69325800-69344800	Weak transcription	Brain Anterior Caudate	brain
16	chr5:69336600-69345000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr5:69342600-69345000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr5:69342600-69345000	Weak transcription	Fetal Muscle Leg	muscle
19	chr5:69343000-69345000	Weak transcription	Fetal Lung	lung
20	chr5:69344000-69344600	Weak transcription	Dnd41	blood
21	chr5:69344600-69344800	Enhancers	Primary T cells fromperipheralblood	blood
22	chr5:69344600-69344800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
23	chr5:69344600-69344800	Enhancers	Dnd41	blood
24	chr5:69344800-69345000	Enhancers	Primary B cells from cord blood	blood
25	chr5:69344800-69345000	Enhancers	Primary B cells from peripheral blood	blood
26	chr5:69344800-69345000	Enhancers	Primary T killer memory cells from peripheral blood	blood
27	chr5:69344800-69345000	Flanking Active TSS	Brain Anterior Caudate	brain
28	chr5:69344800-69345000	Enhancers	Fetal Thymus	thymus
29	chr5:69344800-69345000	Enhancers	Pancreas	Pancrea
30	chr5:69344800-69345200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
31	chr5:69344800-69345200	Flanking Active TSS	Dnd41	blood
32	chr5:69344800-69345400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr5:69344800-69345400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr5:69344800-69345400	Active TSS	Breast Myoepithelial Primary Cells	Breast
35	chr5:69344800-69345400	Active TSS	Primary monocytes fromperipheralblood	blood
36	chr5:69344800-69345400	Active TSS	Primary neutrophils fromperipheralblood	blood
37	chr5:69344800-69345400	Active TSS	Primary T cells from cord blood	blood
38	chr5:69344800-69345400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
39	chr5:69344800-69345400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr5:69344800-69345400	Active TSS	Primary T helper naive cells from peripheral blood	blood
41	chr5:69344800-69345400	Active TSS	Primary T helper naive cells fromperipheralblood	blood
42	chr5:69344800-69345400	Active TSS	Primary T helper cells PMA-I stimulated	--
43	chr5:69344800-69345400	Active TSS	Primary T helper cells fromperipheralblood	blood
44	chr5:69344800-69345400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
45	chr5:69344800-69345400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr5:69344800-69345400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr5:69344800-69345400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr5:69344800-69345400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr5:69344800-69345400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr5:69344800-69345400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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