| Tag | Content |
|---|
EnhancerAtlas ID | HS002-01099 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr1:213499790-213501110 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:213500371-213500392 | TTTTTCTTTTTCTTTTTTTTT | + | 6.09 | | RREB1 | MA0073.1 | chr1:213500944-213500964 | TGTATGTGTGTGTTTTGGGG | - | 7.06 | | SPI1 | MA0080.4 | chr1:213500361-213500375 | TTCTTCCTCTTTTT | - | 6.14 | | SPIC | MA0687.1 | chr1:213500361-213500375 | TTCTTCCTCTTTTT | - | 7.01 | | ZNF263 | MA0528.1 | chr1:213500531-213500552 | GAGGGAGGAGGAGGGAGAAGC | + | 6.86 |
|
| | 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 |
| GH01I213324 | chr1 | 213498112 | 213501390 |
|
Enhancer Sequence | TGAGGCAGAT TTCTACCTCT TTTTTGCTTG ATTCATCTTC ATTGCTAATC ATCTGAAGGC 60
TGCCAAATGT TCACTGACAC TAATGTATTA TAGGTCAAGA GAGGCAGGTC TTCACCTATT 120
ACCCCCCCAA ACAATATGCT TCCCTTCCCT GTTTCCTCTT CAGGATTTTC AGCAATCACT 180
GCCAGATGCA ATCAGACTCC TTGAATAGGA GCAACTGAGG CTTGTTTGTG GCTCGGATTC 240
ATTAGAATCA GGAGGCTGAA GAAAGGAATA AATTACTTAA TTGCACAAAA AAGTTGCAGC 300
CAAAGTGATG GTGAGAGAAA CTGATTGTGT AGATACGCAT TAGGCCACTC TTGGAATGGG 360
GTGTCTTAGA ATAGCTGGTA GTTTGGCCTC ACAGATTCAG ACAGATTTGG GTGTCCTCCA 420
AAACAGATGG CTCCACATAC CATCTATTCT TCTCTTTGTC AGGTTTTACC ATTTATTTGA 480
TCTTGGTCCC TCTCTGATGC TGGTTGTATT AGTTGTAACA CAAATATGCA TTCAGATCAT 540
ATCCATTTAG TCTGGCCTCT CCCAACTTTT GTTCTTCCTC TTTTTTCTTT TTCTTTTTTT 600
TTTTTTTTAA TTTTCTTTTT GAGAAGATGG TCAAGTTGAA TTAAACCCTT GTTGTCCAAC 660
TCTTGAATGC TCCTTCACAT GAAATGCAGG AAATGGGAAG ATTGCACAAG CCTGCAGTGC 720
GGGGGTGTGA GCCCTAGACT GGAGGGAGGA GGAGGGAGAA GCTGCTCAAA TGGGGAAAGA 780
AAGAAAAGAA AAGAAAGAAA GAAAGAAAGA AAGAAAGAAG CTCTATTTTC CAACCACAGG 840
GATACCTTCC TTGCCTCAAA CTAACTCTTA ATCCGTTAAA AAAAAGCACA ATATTATCCA 900
GTGTTGTTCA TACACAACCA AGGAAGAAGA AACAAAACCA TGCAGAGCAG TCTCACAAAT 960
GCTTCCTTCT CTTTTCTCTG GCACTTTGGC ATGTGCCTCC AGCCATGGGG CCTCTGACTC 1020
ACACATTCCA CTCAGGTTTT TGGTCATGTG CCTGACTTGC GGGTGGTCTT AAGGTCTTGA 1080
AGACAGAACT TCATTTTCTC TGTGAAGTTC CTGCATTGCT ACTAGTTGTG TGTGCGTGCG 1140
TGTGTGTGTG CATGTGTATG TGTGTGTTTT GGGGATGGGG TTGGGAAGAG GGAGGAGAAG 1200
GTTCAGTATG AGACAAGAGG CACTGACAGG GAAGAAATTG GGAAATAAAT TATGATTGAT 1260
TTCTATTTGG GAAGAAAAAG TATTCAGAGA GGTAACTTTT CTAATACTGT TGAAAAGTAA 1320
|
