| Tag | Content |
|---|
EnhancerAtlas ID | HS176-39099 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr8:8365270-8366740 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr8:8365684-8365699 | AGGTCAGCCTGACCA | + | 6.54 | | HSF1 | MA0486.2 | chr8:8366391-8366404 | TTCTAGAATATTC | + | 7.22 | | TEAD1 | MA0090.2 | chr8:8365977-8365987 | CACATTCCAT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TAGATAGATA GATAGATAGA TAGATTTAGG AGGAAAAAAG TATAGTCCTT TTAAACCTTT 60
GAATGATTTT TAGAAGCCTA ATAGGGTTAT TAGGAAGAAA AGCATTCATT TACAAGCGGA 120
GAATTAATCT GCAAATACAG TGGTGCAAAA TACCCGATAG GAGAAGAAAA AATAATCTCA 180
TTTGGCTAGG GAAAGGAAGA TGGGCATTTG CTGGATAATA TATATCACTC TATATCTATA 240
ATATGTCTTT TCTTAGTCTT TTTTATTTTT CAACACAAGA GACTATCAGT ACTGAGTCTA 300
ACAGTCTTGG GTGGAAGGGG TAAAAGCTTG GAGGAGGAAG CTGGCTGGGG GCTGCCTGGA 360
TAGGATTCAA GATCATAGAT TAGCAAATTT CCGGAAGGAA TCTGCTGCAC AGTCAGGTCA 420
GCCTGACCAC TTTGCCACCC GCAGCTTTTC TACTGATTAG ATTTGTAAAT GGGCCAAGAC 480
CTAGACATTC ATCCTGCAGC AATTCAGCAA GGCAGACACG GAATTAAGTC TGAATGGACA 540
TGCTCAGGAG CTCCAAACCA AGCAGGAGAG AGGCAAGGAA TCAATGAACC TCTTGGAATT 600
TATATCAAAT GGACAAAAGA GCAGGCAGTA TGTGGGCCTC TATAACAATG GCTTTGTTCC 660
ATTGTTAACA GTAGTGCTAC CATCATGAGC TGAGCATGGA GGTAAGCCAC ATTCCATCGC 720
ACTCTTTGCT GGGTGTGATG AATCTAGAGT TAGCAGGTGT GTGTTGACAC TCAGAGAGAA 780
GCAGTCTTGG TGAAAAGACC TCTAAGCTAT TGAGGCAGCT ACTATGTCAG AACAGAGAGA 840
TTGACTCTAG GAGAGTTGAG GTTTACCAGG GAATAGAGAG GAAGTTAGAA GGACCAATGT 900
GGCCTTCCTT GCAAAATTTA GAGAGTGGCT TTTCTGTTAA AACAGGACTA GCTATTGTCT 960
ACGGTAGTGT TTCTCGAATT TTAATATGTG CATGAATCCC CCAGGGATCA TATGAAAATG 1020
TCCAGCCTTG ATTCAGTGGC TCCGAAGTGG CCTGAGATAC TGCATTTCTA ACAAGTTCCC 1080
CAGAGTTGCT GAGGCTGCTG AAAACAAACC ACAACACTAA ATTCTAGAAT ATTCCCTAGA 1140
AATATTTTTA AGCTGAAGAG AAGACAAAGA TAATTAGCAA GCTAGTTTTT CCTTGGGCCT 1200
GAGTGAGGCC AGGATTGGAT TAAATTATGA TTTTTATCTG GTTAGGGATC AGTGCTAAAG 1260
GTAACAAACT GTGCCTGGAT GTGTGTATCA CTTTAGCATT TGCTCTAATA GTGGTCAGTT 1320
TGTAAATACA GTATTCTTAT GTTTATTAGC TCATTTAGAG AAAAGTATAT TCTTTAGAAA 1380
ATTATTTGTT GCATAGTAGC AATGAATAAA TGGATAAATA AACAACAAGT GAAAATGCAT 1440
TGTACATTCC GACTTAGCAA AGCAAACGAG 1470
|
