| Tag | Content |
|---|
EnhancerAtlas ID | HS052-37635 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr8:124006460-124008030 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr8:124006807-124006818 | GGATGACTCAG | + | 6.32 | | JUNB | MA0490.1 | chr8:124006807-124006818 | GGATGACTCAG | + | 6.14 | | ZEB1 | MA0103.3 | chr8:124007520-124007531 | GGGCAGGTGGG | - | 6.14 |
|
| | 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 |
| GH08I122994 | chr8 | 124006391 | 124008117 |
|
Enhancer Sequence | CTAAAAAATC TGGTGGTTAT TGTGATAATT AAATGAGATA ATGTACTAAT AGATGTGGTA 60
GTGCTTTGTC ACAGCAAGCA ATTATGGTGA TGAGAATGGT GACAATGATG GATAATATAG 120
GTGGTTGTCA TCTGGCCAGT GTCCATAAGG TAGAAATATA GTGTCTTTCC CATTGAGCTT 180
TGCCATTCTA GACCCAAATC CTCCAGCCTC AGCATTCCCA GTTCCCTAGA CTAGAGGTGG 240
TCCCACCTAC TGCAAGCACT TCATCTTTCT CCTTCCCAGG ATTCGGTCAT TGTCTGCAGC 300
AGCTGTGCCT GTGGGACCTG AGCCCGCTGT TACGAAGGAA AGCATGGGGA TGACTCAGGG 360
AGGGTACATC AGAGCAGTGT GGGTGGAAAA GCCTTCACTG ATGAGTTACT TTCTGAAGTA 420
CTCTTGTATT TATTTTCTTA GATATCTGAG AAACACATCT GCAGTGCCAA AACATTCATT 480
CAATACTTAC TTAATGAATG CCTTCTTTGT GTCAAGCACT GTAATTGCTG GGGAAACAAA 540
ATTGAATGAT ACTTGCTCCT ACCCTCAATT GACCCTGCTG GTCTGTGCCT TCAGGAGGTT 600
GTAGGCATTC CAGGACTTAG TCCAGTTACC CAGGGCCCAG CACAATGTCA GAACATGACA 660
GGTGCTCAGT TCACTTCTGT TGAACTGATG GATGTTAGTC TAATGGGGGA AGCAGGGAAG 720
TTATCAACAA CTTTAGAGAA AACTGGGAAA ACAGAGGGAG AGAGCACGTA CTGCAAAACA 780
GAGCTCATGA TCAGCTCCCT AGGGGAGATG GCACCTAAGC TGAGTTCTGA GACAAACAAG 840
AATAAACCAC AAGAAAAATT AGGTGGGAGG GGACAGAGGT TGGCAGAAAG CCATCTGATG 900
CAAACTTAGC TTTTCCTGTC TTCTGGCTTT CTCTTCTACT TAACTTCCAC CTGCCTCTCC 960
CTGCACAGTG GATGAGGGTT TTGTTCTCCA ATGGGAAAAT AAGCTTCACT AAATACCACA 1020
GAAACATCAC TGTGAAGCCT GCTCTGGTCT CCTGTATGGA GGGCAGGTGG GAAATGACGG 1080
TGGGCCTCCC TGCAGGCTTG ACAAGCCAAG AAGAAAGGGG GCATCAGATG CCGACAAGGA 1140
GCAGGGACCA GAGAGCAAGA GAAGGTGGAG AGACTGCGGG CAGAAGCAGC TCCCATTCCT 1200
GCACGCACTC TGTGAGGAAC ACAGGGCCAG GGGCAGAGTC CACAGAGTCC CAGAAACAGC 1260
CTCTCCTCTG GGCTCAGGTT AACATTGGAC AAAGGCACCG AGCCTTACGT GCCTAGGATT 1320
TCAGAGCAGG TGACGCAGCC ACTTTTGACA CCTGGTGCCT GTAAATCAGC CTGGAGCTGG 1380
GCTCAGGGCC AGCTGCATCT CTCCTGGAGC AGAGCATGTG CTCCTCACTG CTCAGGACAA 1440
ATCCAAACCC CTCAGTATAA CATGAGTGGC CTCCACCTAC CCTCCAGCTC CATCTCTACC 1500
CACTTCTCAG CCTTCATCTA CACTTGCCTC CAGTTCCCCA AACACCCCAT TTCTCTTCCT 1560
CCAGACCTCT 1570
|
