| Tag | Content |
|---|
EnhancerAtlas ID | HS176-11600 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr13:75824510-75825770 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr13:75825466-75825479 | TTCTGGAATCTTC | + | 6.2 | | SOX10 | MA0442.2 | chr13:75824560-75824571 | AAAACAAAGGA | + | 6.32 | | Sox3 | MA0514.1 | chr13:75824560-75824570 | AAAACAAAGG | - | 6.02 | | TP63 | MA0525.2 | chr13:75824615-75824633 | GATGTGTTACAACTTGTC | - | 6 |
|
| | 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 |
| GH13I075250 | chr13 | 75824641 | 75825780 |
|
Enhancer Sequence | CTGAGTTGAG TCTCTCCACT AAGAAAATAT GCTAGTGCCA CAATAGGAGA AAAACAAAGG 60
AACAGTCCCT CTTCAATAAT TCTGTTTGAT TCCTGTTTCT GTCTAGATGT GTTACAACTT 120
GTCCACATAC CTTCACAAAT CAGAAAAGAA CTAAATAGGA TTATATCAAC ATTTGCACTC 180
TATGTACCTA TTCTGAAGAA TAACACAGGA AAGAGATTAC TTGGAAGGTA TATTTAAATA 240
CTTAATTTCC TCAATCGAGT TACAAGAGAA ATGGACTGAG AATTAGGTCT CTGGGCTTGA 300
GTCTATCAGT GATGGGGATT ACTTCACTTT TCTGGAATTT CTTTTCTCAT TTTCTTAAAC 360
ATATGACTAT GAAATGTATG GCTGTCCGCC AGAGAATCCT ATCAGACAGA ACCCCCGAGA 420
TATTTCCATA TATATATATA TATTCTTACC TCTGGGAGAT TCTTACCTGC CATAATTGGG 480
AGAAGATGGG GTTGATCAAG AAGAGGAGGT CTGTCATGTG GCTTTTGACA CCGCGCCCCT 540
CGTCCACCCC ATCCTCCACC ACAGTTCCCA GCCAGTTTAG AACCGCTGGA CTAGATAAAT 600
CACCAGGGTT CTTTCCAACT AAAACAATCT CTGATTCTAT GACTCATTGA ATCATGAAAT 660
AATCTAATAG ATGTGACCTA ATACAAGGGA TCTCTTGCCT CTGAATTCCA TGACATTTGA 720
CCACAAATAG CCTATAGAGG ATAATGAAGT TTCTGTGGCT GAGCACTCCC ACCTCCCTGC 780
AAAGAAACCT TTGCACCCTC CCTTTAACTT ACTCAAAGCA GTTTCAAATA GGAACCAGAA 840
TCAAATTAGA AAAGTAACCT AGCAGACAGA AATGTGCCAC GCATTTGCAG AATAGGAATA 900
TAGAAAGTAG GAAAAGCTGT TTTTACTATG AAATTTGTAA AAGCAACTCA CTTCCATTCT 960
GGAATCTTCT TCCTAATGAA ATCATTTTTC TCATCCGCCC AGCTGTGCAG GAAGTGTGAG 1020
TTATCACAGT TCCCACTGTT GTAACTCCAG TCCCACGAAG TCAGAGGAGT AAATGAGCTG 1080
CTCCCTCACC ATTTTGAACT GATATAGGGG ATTTCATATT TTAGTCAATC AAGAGCACAT 1140
TCCGCATATG TTGTCTTTCT CAAATGTTTG GATATCTTTT TTTTCTTTTT TTTTTCTTTT 1200
TTTTTTGAGG CAGGGTCTCA CTATGTCACA CAGGCTAGAG TGTAGTGGTG CGATCTCAGC 1260
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