| Tag | Content |
|---|
EnhancerAtlas ID | HS093-27956 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr7:17728930-17730150 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr7:17729284-17729295 | TCAAGGTCATT | + | 6.32 | | Esrra | MA0592.2 | chr7:17729283-17729294 | GTCAAGGTCAT | + | 6.32 | | Esrrg | MA0643.1 | chr7:17729284-17729294 | TCAAGGTCAT | + | 6.02 | | NFE2L1 | MA0089.2 | chr7:17729881-17729896 | CCATGAGTCAGCATT | + | 6.34 | | Nfe2l2 | MA0150.2 | chr7:17729879-17729894 | GGCCATGAGTCAGCA | + | 6.08 | | REST | MA0138.2 | chr7:17729163-17729184 | TTCAGCACCTAGGACAGCCAA | + | 7.34 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_36076 | chr7:17728819-17730898 | HMEC | | SE_64670 | chr7:17729085-17730654 | NHEK |
|
| | 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 |
| GH07I017689 | chr7 | 17729564 | 17730645 |
|
Enhancer Sequence | AGGGCTTTCT TTAAATGCTC TGGACAATGA GTGGAGCTAG GGTCTTCATA GATCCTGGGG 60
CCGAGGTAAA GAAAATAGAA ATAGAAATTT CCACCCACCT TACAGAATGG GAACTTAGGT 120
TAAATTTGAT GTAAATAAAT AAAAGAAACA TGATATGCCT TACACCTTGT ACTGAAGAAT 180
AAAATTAATG CCTCTTCAAT TTATATGATA CAATAGGAAT GATAGGAGGC TCCTTCAGCA 240
CCTAGGACAG CCAAATACGA AGGTCATCCA TCTGTGAAAG GAAAAATTCC CAACAAGACC 300
TTCAGCACAC ACCAAATAGA TTTAATTTAT AGTTGACATT GGTTCACAGA ACAGTCAAGG 360
TCATTGGCAC CTTAATTACA ACACACTTGG CCCACACTCC TTACCCAGCA GGTAATAGCA 420
CTAACATGCA TGATGAAACT CCTGTCCATC ATCCAAATTC AAGATGATAA GTTTTGATTC 480
GGTTACTGAG ACTATTATCG TCTGTTTTAT CTTGATGAAA TAGTGACTAC AAACACAGCT 540
CCAGGCTAAT TTGGAACAAT GTCAACACCT AAAAAATTAT CTCCTTGGAA GAAACGTGGG 600
TAAATTAGAA TAAACCTTTT ATGCATTAGT AAGTATTAAT GTACTTAAGG TGATTCTTGC 660
TGGTGTGTGA TTCCAAGATT TAAGCAGGAA TATTTACATT CTTTAACACT CTTACTTTGC 720
TCCATTGAAA GACTTTCCCT CAAGCTCCCA CTCCTGTGTC CCCTGAGACT ACTGTAAGTT 780
TCTAGAGCTG ATGAAACCAC CTGTAGGGTA GAAAGACCAG AATAGGGCGT GTGGTTTAGC 840
AAGTCTTTTC TAGAGTTATT CTTGGCCCTG AGCACCACTA GCATGGTGGG TGTTTCTGGC 900
TGAATCTGTC TGGTTGTCCT CATGCTGCAC ACTCTGACGG GTGACCTGAG GCCATGAGTC 960
AGCATTGTGG TAACATTCCT TCTCATTACA CCAGCCATTC TGCTTGAGTA GTCCTCAGAA 1020
AAGGGAACCA TTTTTTAGGT AGGAAAACAA GCTTCTCGTT GTGGTCTATA ACCTCTTCTC 1080
TCCTCTGGGT TCAGGGCGGG AGAGTTACAA TGCCCAGAGA AGGGCATGCC TCTTCCAGCC 1140
CCCTAATACA TATAACCACA TTTGATTCTC ATCATAACCC TGCAATGTTG TTCCCAGCAA 1200
GATGGTCTGT CACAGAATCC 1220
|
