| Tag | Content |
|---|
EnhancerAtlas ID | HS176-38478 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr7:124701320-124702470 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr7:124701852-124701864 | GAATGTTTTTTT | + | 6.52 | | JUN(var.2) | MA0489.1 | chr7:124702266-124702280 | AGAAAGTGACTCAT | + | 6.93 | | ZNF263 | MA0528.1 | chr7:124701353-124701374 | CTCCCCTTGCCCTCCACCTCC | - | 6.11 | | ZNF263 | MA0528.1 | chr7:124701350-124701371 | TCCCTCCCCTTGCCCTCCACC | - | 6.34 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH07I125062 | chr7 | 124701601 | 124701750 | | GH07I125061 | chr7 | 124701855 | 124702850 |
|
Enhancer Sequence | CGCATACATT AGGTATTTGT CCTAATGCTC TCCCTCCCCT TGCCCTCCAC CTCCCTGGCA 60
GGCCCTGGTG TGTGATGTTC CCCTCCTTTT GTCCATATGT TCTCATTGTG CAGCTCCCAC 120
TTATGAGTGA GAACATGTGG TGTTTGGTTT TCTGTTCCTG TGTTAGTTTG CTGATAACGA 180
TGGTTTCCAG CTTCATCCAT GTCCCTGCAA AGGACACGAA CTCATACTTT TTTATGGCTG 240
CACAGTCTTT TCTTTATAGT ACATAGCTGG ATCGTTACTC ATTATGTTTA TTGAGTTCCT 300
TCTATGGGCA GAATATCTGT AAAGTATTCA GAACTAAAGG AGGCTTTTAA AAGTAAATAG 360
AAAGCAATGC TTTTGAGAAA TAGCCACTTA ATTAGTGAGA TTGAATCAAC ATATTCAGGC 420
AAGCAGTAGC AAAAAAAAAA AAACCCCACA TTTTATAGAA CTAAGTAATA TAATGTAAAA 480
TAATTGTGGG ATGGATTAGT GCCTGTTTGA TTTCTGATCA ATGCTTTTGT TAGAATGTTT 540
TTTTAAGAAA AGCCTAAATA TGCTGTTTAA GACTGATAAA AATCTTACCA TGTAGATACT 600
ATTATCCTTA CTTTTTGATA AATGAAGAAA CTAAATCCTG CAGAGGTTGA CTAATCTACC 660
CACTCACACA GCTAATAGGC CATGGGACAG GATTTGGATT TAGATCCATT CTGTCTCCAG 720
AGCCTGAGCA CTCTCCACTA TGCCAAACAG AACTCCAAAA CCCTTTCAAG ACACACCTGG 780
CTCCAAGCTT GAGCTCACAC TCATTTTGTT TGTCTCCTAA AGTGAAATTT TAGGTTGCCT 840
GTCTTGACTC TCTTCAGATA AAAATCCCTC AGAAAATTTT TTAGAGTCAG AGTTGAGATT 900
GATTTCTGTG ATTCATTTGT CACTGTGAAA AGAGATTAGG GCTGAAAGAA AGTGACTCAT 960
ATGATGGCTC ATGTTCACTG CAGCATGACT GGCAGCTTCT AGAACAGAAA AACAGACTTC 1020
TCCTTTTCTT TGGGGAGTAA GCAGCACGGG GAAATTTTAT TCAGTAAAGC TGATGACAAT 1080
TTTCCTTTAA ATTGGACACG AATTCTCCTA GGAACACTGC ATAGTAATAT TCCTATGCCC 1140
ATAAAATTTC 1150
|
