| Tag | Content |
|---|
EnhancerAtlas ID | HS092-04002 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:182317900-182319340 |
Target genes | |
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 | TAATTATCTG CCTTCTCCTT GCTAGAATGT AAAATCTTTG AAAACAGAAA TGTCTGTTTT 60
GTTCTCTTGT GTATATCAAG CACCTAGAAG AACCTCTGAT AGGTACAATT GCTTAATAAA 120
TGCATGAATG AATAAAAGGA GCAGCCAAGG GTGCAGTGTG CTCTGAGCCA GCCGCTGGGG 180
GCTCTTTCCA TGCAGTGTCA CTGTTTTCAT CACCCTCTTT CTCCAGCCCC TCAGGATGCC 240
ATGGTTGGCA AGCCCATGGG TCTGAGTCAG TACAGAGCCA GGCAGGGTTT GTCCCTGGGC 300
TTCATGGATT CTCGGAAGGC AAACAGTGTC AGAAACATTC TTTCTAGGAC TCGTGAGTTC 360
AGCCCAGGCC AGAAATAGCA CCCAGCCATG TGCCTTCTAG TATTTCTGCA CATCAGCTTC 420
TCCTCCCACT GGAATGGCAA AGAGGAGCGT GGAAGGCTGA AAACAACTCC AGGCCTCAGG 480
AAGAGCCTCA AAGATAGGGC AGAAGATGAG AATGCACTGC TTTGCATGTC AGTTTCCCTG 540
CCTGGTGCCA GCCCAGGCCC AGCTGTGTGC TTACCTCATG GGAGGCCTGT AACCTGAGTC 600
AATTTTGTCC TTGCCCCTTT GGAAGGCCTG CCTATTACTT ACTTGGTGTT GCCAGTGAGG 660
TCTCAGGGAA CAGACGTCAC ATTGCCCATC TTCTAGCTGT TCTGGCATAA CTAACCAAGA 720
CTGACTAAGC AAGCACAGGG CTCAACAGTT TTACCTTCTG AGCAAACCTA GTGAATCGCA 780
GAGAGGCGGG CCCCCTTCTC CCCTTCCCTC AGGGCAAGGA AGGCTAAGGT GGAGGCTACT 840
TTAAGAGGGG GCCTTGCACC AAACATTTTC TTCTAAACTC TAATGAGTCT TGGAAAATGC 900
TCCCTGAGCT TGGATGCCCA AATAATCATT GTCCAGTCAG GAGGTTGAAA GCATATTGCC 960
AGCCCCTTGC CCCTCCCCCC ACCCAAAAAA AACAGGAAAA ACTTGAGGGC TTTTCCAGCC 1020
CTGGACTTAA GGTGCTTATC TCTTTCCTTT GGTTCCTTTT TGTTTGGGTG GAAATTGCAA 1080
ACAGCAACCA AGATTAGCTC CCATATTCTC CCAGGTTGTC ACTGGGCAGG ACTATGTCAG 1140
GGCTTTCTCC CCCACCACCC ATTTCCAGGG TAGTCCAAGA AGCACATTTC AAAGCCCTTT 1200
CTTCTCTTCT TCCCACCTGT CCCCCTGCCC CTTATTGACA TCTGGTGGAT AGATATTCCT 1260
TAGCCAGTCA GAATGAGTGG GGTCCATGTT GATCAACTGA GAGTAAGCCA AGAATCCTCA 1320
AATCAGAGGA ATCTAAACCT CCAGTCATTA CTCAGGGTTT CCAGAGTTTT CCTGAACCTG 1380
GACCAATATC CAATGATCCC CATCACCACC AGTACCTGCT GGGGTCCCCC AATCCAGCTA 1440
|
