| Tag | Content |
|---|
EnhancerAtlas ID | HS148-17358 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr7:121144180-121145590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr7:121145272-121145288 | CGCTATGTAAACAACA | + | 6.49 | | Foxa2 | MA0047.2 | chr7:121145273-121145285 | GCTATGTAAACA | - | 6.32 | | JUN(var.2) | MA0489.1 | chr7:121144773-121144787 | ATGACTCACTCTCT | - | 6.21 | | SRF | MA0083.3 | chr7:121144275-121144291 | TTACCCTATATGGTCT | + | 6.07 |
|
| | 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 |
| GH07I121503 | chr7 | 121144050 | 121145693 |
|
Enhancer Sequence | CCAAGATGGC GACAAAAGTG ACCTCTGGTC ATCCTCACTG CTACACTCCC ACCAGCACCA 60
TAACAGTTTA CGAACGCCAC AGCAATGTAA GGAATTTACC CTATATGGTC TAAAAAGGGG 120
ATGCATAAAA ATTCCACCCC TGGCTTAGCA TATAATCAAG AAACAACCAT AAAAATGGGC 180
AACATGCAGC CCTCCTATGA AATAGCCATT CTTTTATTCC ATTACTTTCT TAACAAACTT 240
GCTTTCATTT TATGGATTCA CCTCAAATTC TTTCTTGCAT GAGAACCCTC TCTTGAGACG 300
TGGATCTGGA CCCCTTTCTG GTAACACAGG TACTCAGGGC CCCACTTCTT TTCTCGGTTT 360
CAGTGTGGAT GTCCCACTTC ATAGCCTCAA GCTATGGAGC CAATACTGAT TGCTCTCCTG 420
GGCAGTAGAA ACACGGGGGT TGTAGTTCCA CCTGGCTTCA AACCCCCAGG TCCGCTGGAT 480
GTTTATCTAA ATGCGGTCCT TACAAACAAG GTTCTTTTAA ATGGAAATCT AGCAGAACCT 540
TCTCCTTTAG GCTAAAACTG TTCCACCAGG CAGTCTCCTG ATGCCAGGAT CTGATGACTC 600
ACTCTCTGCT TCCCGGTTCC TGTGTCCATA AATTCCTTGA ATTAGCTAAA GAATGCAGTC 660
CAGGCAAATT CTAGTTTCTT ACTCAGACAC TTGACTGAAT ATCTCCTTTA CTCTCATTTC 720
TTCTTTCTGC TTCTTTTATC ATTTCCCTAA ATTTATATTT TCTACTCCTA CACTTTATAA 780
GTTGCTTTTC TCTCTGTAAA TACAAATTTC ACACATTTTC AGAACCTACC AAGTATTATA 840
CATAGGCTTC TGGGGGTGCT ACAGCCCATT CGACTCTCAC AATTAAGACT GTGGTGCTGT 900
TCAAACCAAA CAATGTCAGG TTGTTAACAT CACTTACATG GTTAACACAC TTGATTAGGA 960
GTCAGTGTCT TAATTGTGGA AACAATTCAA AATTTTCTTG TATATGACAC AACCAGTGAG 1020
GTATTCTTTG GAATTTCCAT GACCATGTTT CAGGAAGTAC AAACTTTGCT GCTAGCATAT 1080
TGGTCCACAA ATCGCTATGT AAACAACAGA TGCAACCAAT CATGATCAGC AACCTTCACA 1140
TCACCTCTTT AAAAGCCTGT CAGTGATTGG TCACTGCACA TCTGTTACTC AGTTCACTCA 1200
CAGAAAGCAA AACATGGAGT TGTGTTGCCT CCTGGTTTCC CAACAGTAGA GAGATGCTGT 1260
AAGCAAAGTA GTTTAACTTT TAAAGCACTA CTACTGTTAC CCTCATTCTC CTGGTGACTT 1320
CTGAATGTGG AAAATTTGCT TTTTAGCACC AACAGAACTG CATTATCCAG CCAATGGGCC 1380
AAGGGAGTTG TTTTAACTTT TAAAGGCTCA 1410
|
