| Tag | Content |
|---|
EnhancerAtlas ID | HS095-08226 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr13:31292620-31294070 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DUX4 | MA0468.1 | chr13:31293926-31293937 | TAATTCAATCA | + | 6.14 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_37797 | chr13:31292228-31294599 | HSMMtube | | SE_59818 | chr13:31293174-31321295 | Ly4 | | SE_63988 | chr13:31292247-31295301 | HSMM |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I030718 | chr13 | 31292497 | 31295337 |
|
Enhancer Sequence | CCCCCTTCCT CCATCCTTTT CTCCATTGCA TACCCATCCA CTGTGCCCTT TGGAATGCTC 60
ACACCATGAA CTGCAAACTC TCGTGTGGCT TCAGCCTCTT CTCTGAAAGT TCCTCTCACC 120
TATTACTTTC TCTGGAACCT GCCATCCCTG CCACCTTCTC AAAAAAGGCC TTTTATTCTC 180
TTCATTCCAC AAAGCTCAGT GTCAAAACAT GGGGTTTACA CTGGAAGCTG AGGTCACATC 240
AGTAGCCGGG ATCAGGGTCG CCCTAGCTGC CCAATGCAGC TCCCAGGCCT CCTGTAAAAC 300
CTTGACCTTT GAGGTCATGA CAGCCCTCTC CTGCTATGCT CATAGCTGAC CACTGAACTC 360
CTGGACACTC CCTCCCCCAA GTTCACAGAG AATGTGGGCA CATGCCTTAC AGTCTTCCCT 420
TGATCCAAAC TACTGCCTTC ATCTTGAGTG ACAGCAGCAT CTTTTGGATG TCTTGGCCTG 480
TCTAGCTTTA TTTTTTTGTG TTCTGCCATC AAGTTGCTAC TTCTGTTGCC ATCGTGCCTG 540
TCAGCGCAGT GCAGGCTGTG GTGAAATCCC ACGAACTCAG GCATCACACT GACCGGGTCT 600
GAGTCCTGTC TCAGTTGTCA GCTAGTTGTG CAATGAAGGG AAAGGGACCT ACACTTTCCA 660
AGCCTCAATT CACTCATCTA TGGCATGGTG ACAATAATGG AGGTTGATTT AAAGTCCTTT 720
GTAAGAATTA AGAGTTATAA TAGACATAAA GTGCTGTATC TGGTATACCT AGAAAACATT 780
CCATAAAAGT TAGTAATTGT TGGTCATGTA ATGATGACTC TCTAGGCTAG GATTTCAGCT 840
TCATTGCATG CACATGGTGC ACTCACAGGG CGTGACCTCT CTCTGTCTCA GTAACCTCAT 900
CTGAGGACCG GGATAATCAT ACCGCTTCAA AGGGATGTCA TAAAGATTAA ATAATATGTG 960
TAAGGCTGCT TGCATTTAGC TGCATTCAAC AAATATTTCT GTATCTTTCT CCTCATTTCT 1020
CCTTACTTTC TTGCTTATTA TCTGCTCTAG GTATAGATTT CAGAGAACTA AGCTTGTTAC 1080
AATCCTTCAT AAAATAACCA GGTTGGTTAG GGCATTTCCA AGAGTCAATA CTGTTTAGTG 1140
ACTATTCTCT GTTTAATCTA TTTTGATTGT CCAGGGTCAT CTTTTGCTAT GTCATAGGTT 1200
GTTGGCTTCT TCTAGAGAAG TGAGACGATG GACAAGTTCC AAGTGAGTGA GGCGACTGGT 1260
CAGGATATTC CGCTGAAAAA CTCATGTCAG TTCTAATTCG TGATTGTAAT TCAATCACAG 1320
CCTGAGAACA GTAGGACTGT AGTTCAAATG CTCTGTTCCC TTTTTTTTTT CCCAGAGGAT 1380
AATTTTTTTT TTTCTTTGAG ATGGAGTCTT GCTCTGTCAC TAGGCTGGAG TGCAGTGGCG 1440
TGATCTCGGC 1450
|
