| Tag | Content |
|---|
EnhancerAtlas ID | HS052-03009 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr1:182317950-182319340 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:182318689-182318710 | GCCCCCTTCTCCCCTTCCCTC | - | 6.1 |
| | | 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 |
| GH01I182348 | chr1 | 182317312 | 182320459 |
| Enhancer Sequence | TGTCTGTTTT GTTCTCTTGT GTATATCAAG CACCTAGAAG AACCTCTGAT AGGTACAATT 60
GCTTAATAAA TGCATGAATG AATAAAAGGA GCAGCCAAGG GTGCAGTGTG CTCTGAGCCA 120
GCCGCTGGGG GCTCTTTCCA TGCAGTGTCA CTGTTTTCAT CACCCTCTTT CTCCAGCCCC 180
TCAGGATGCC ATGGTTGGCA AGCCCATGGG TCTGAGTCAG TACAGAGCCA GGCAGGGTTT 240
GTCCCTGGGC TTCATGGATT CTCGGAAGGC AAACAGTGTC AGAAACATTC TTTCTAGGAC 300
TCGTGAGTTC AGCCCAGGCC AGAAATAGCA CCCAGCCATG TGCCTTCTAG TATTTCTGCA 360
CATCAGCTTC TCCTCCCACT GGAATGGCAA AGAGGAGCGT GGAAGGCTGA AAACAACTCC 420
AGGCCTCAGG AAGAGCCTCA AAGATAGGGC AGAAGATGAG AATGCACTGC TTTGCATGTC 480
AGTTTCCCTG CCTGGTGCCA GCCCAGGCCC AGCTGTGTGC TTACCTCATG GGAGGCCTGT 540
AACCTGAGTC AATTTTGTCC TTGCCCCTTT GGAAGGCCTG CCTATTACTT ACTTGGTGTT 600
GCCAGTGAGG TCTCAGGGAA CAGACGTCAC ATTGCCCATC TTCTAGCTGT TCTGGCATAA 660
CTAACCAAGA CTGACTAAGC AAGCACAGGG CTCAACAGTT TTACCTTCTG AGCAAACCTA 720
GTGAATCGCA GAGAGGCGGG CCCCCTTCTC CCCTTCCCTC AGGGCAAGGA AGGCTAAGGT 780
GGAGGCTACT TTAAGAGGGG GCCTTGCACC AAACATTTTC TTCTAAACTC TAATGAGTCT 840
TGGAAAATGC TCCCTGAGCT TGGATGCCCA AATAATCATT GTCCAGTCAG GAGGTTGAAA 900
GCATATTGCC AGCCCCTTGC CCCTCCCCCC ACCCAAAAAA AACAGGAAAA ACTTGAGGGC 960
TTTTCCAGCC CTGGACTTAA GGTGCTTATC TCTTTCCTTT GGTTCCTTTT TGTTTGGGTG 1020
GAAATTGCAA ACAGCAACCA AGATTAGCTC CCATATTCTC CCAGGTTGTC ACTGGGCAGG 1080
ACTATGTCAG GGCTTTCTCC CCCACCACCC ATTTCCAGGG TAGTCCAAGA AGCACATTTC 1140
AAAGCCCTTT CTTCTCTTCT TCCCACCTGT CCCCCTGCCC CTTATTGACA TCTGGTGGAT 1200
AGATATTCCT TAGCCAGTCA GAATGAGTGG GGTCCATGTT GATCAACTGA GAGTAAGCCA 1260
AGAATCCTCA AATCAGAGGA ATCTAAACCT CCAGTCATTA CTCAGGGTTT CCAGAGTTTT 1320
CCTGAACCTG GACCAATATC CAATGATCCC CATCACCACC AGTACCTGCT GGGGTCCCCC 1380
AATCCAGCTA 1390
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