| Tag | Content |
|---|
EnhancerAtlas ID | HS092-07411 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr10:99308480-99311020 |
Target genes | | Number: 18 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2A | MA0003.3 | chr10:99309259-99309270 | AGCCTCAGGCA | + | 6.32 | | TP53 | MA0106.3 | chr10:99309928-99309946 | AGCAAGCCCAGACTTGTC | + | 6.28 | | ZNF263 | MA0528.1 | chr10:99309140-99309161 | CCTCCCCTCTCCAGCTCCTCC | - | 6.51 | | ZNF263 | MA0528.1 | chr10:99309143-99309164 | CCCCTCTCCAGCTCCTCCTTC | - | 6.78 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr10 | 99309266 | 99310463 | | chr10 | 99308900 | 99309116 | | chr10 | 99310484 | 99310599 | | chr10 | 99309400 | 99310992 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I097548 | chr10 | 99308661 | 99310890 |
|
Enhancer Sequence | CTGAGATTGC GTCACTGTAC TCTGGTCTGG GCAACAGAGC AAGACTCCGT CTCAAAAAAA 60
GACTAAACGA AAACCCTAGA GTTAGATCCT GAAGATTTGG GGGCTCTGTT TGTAATTGAT 120
ATCAGATAGG CCAGTTTTCC TCTGGAAATG GGTCGGGGGA TGGCTGGTCA GTGCCCAGCT 180
CTGGGAGACC ACCCTTCCCC GAGCCCGGCC AGATGTGGCC AGGGCCCCCA GGCTGGACTC 240
ACGGACCAGA GAGCAGAAAA AGGCCTGCTC TCCCTGAGCC CAGCCAGGCA GCCGACCCCG 300
TGAATGTGTA CGTTGTATGC AGCACCATGA AAGCACACCC TGTCTCACGC ATGTGTGCCC 360
CCTTGTCCGT ATCTGTGGCT GCCCGCACAC TGAGGCCTTG GGTAGGTCTG TTTCTCTTGG 420
CTGCAATTTT GTCTCTCTCA TGGCCACAGA GGATCCGGGC CTGCCTCCTC CAGCAGGTTT 480
CCTCACTGTA CACCTACCTC AGTGACTGGT TTTGTCCCTC CTGGACTCCC ACCTCCACCC 540
ACTCCCTTTC TTTCTGCCTC TTCCTATTCA GTGAGGCTTG TTCACAAAAC ATAGTCCTCT 600
GTTCCCCCTT TGCAGGGGTT TCTTGCAGAC AGCTCTGTCT ACTCTCCCAT CTGATCTGTG 660
CCTCCCCTCT CCAGCTCCTC CTTCTTTTCC TAAACTGCCT GCCCATTTCA CTCGCCCGTG 720
CAGCATGCCA GGCATTAACT CTGTCTGTAG GATCAAAAAG ATGAACTGGA GGATGTCCCA 780
GCCTCAGGCA GACAAACAAG ATCATTGCAG AGAATTTCTG TTGCCATGGG CTGGGCATCA 840
TCCTAGAGCC GAGAAGGGGG CTCTCAGGGG TGCCACCCTG CCTTGATCCT TCAGCTCTGC 900
TCAGGACCAC CTGGGACCCA CTGTACCTCT AGAGATGCCC GGTAAGAAGC CTGGCCCATC 960
ACTTAGCAAC TGGCTCCACC CCTTTCCCTC CCTGAGCTGG GGCCCGAGAG GAGGAAAGGC 1020
CCACAGGCCT GTAAAGAGGC CACCAAATCC CAGAGCATGG GAGGCCCCAG CTGACCAGAG 1080
CTGGGCCAGC ACTTTCCCTT CAAAAGTTAC CTAGGCTCTG AGGGTCATCT CTGCTAAGTC 1140
TAACTATAAA TATCGCGCTT CCTGAAGGGA TTACCTGGGC ACCACACCCC CTGGCTCCCC 1200
CCTCCCCGCC TGGGCTGATC CTTCTTCTGG GCCCTGTGTT CTTCCTGACC CCTTGTTCCC 1260
GCTGCCAGGT GGGACACTTC AGACTACCTG TGTTTCAGCT GTGACTGCTG GGGTGGGAGG 1320
AGAGAAACAA GAGATTCGAG TCTGTATCCT GGCCAGAGGG CCCTTGCCGG CCAGCTGTTG 1380
GGACAAGGAG GCTCTTGTTC CTGCCTTCTC CCGTCTGGTG TGAGAGCCGT GTCTCTCACA 1440
CCAGCCAGAG CAAGCCCAGA CTTGTCACAT AATCGGTGCA TCTGGGAAGG ACACTGTTGG 1500
CCCCATCCCT GGAGTAAGGG CCTGGGGACA GAACTTGGTA ACCGAGTGTG GAACAGCTTG 1560
GGGATTGCCG CAGGTATAAA TAGGGCTGTT TCCTGGCTTG GGTGGCCTGA CTGGGGAAAT 1620
CTCTGCTCCC TTTGGCTGGT CTCAGATTTG GTGTCACATC CCAGTGGCTC ACTTATTCCA 1680
GTCCCTGAAG TCACAAGAAC CATCTCCTGG GGTCTGAGAT CAAGAATTGA AGGAGGGGCC 1740
AGCCCGCTGC AGACCTCTCC CCTGCCTCCG CCTGCCTCCC TGCTGCTGCA GGAGCTGTAA 1800
CTCCTCCACC CCTCCCCACC TGCTCACGGC GCCTCGGTCA GTTCCTTTCT CAATTCAGCA 1860
GGTACTTGCT GAGAACCGCG CTGGGCCAGG CACTGTGTGA GGCAGTGGGA TCTATTCAGC 1920
TAGGGTCTGC CATCCTTCCT TGTGTTTTTG GAATCTCCTC TTCTGTGTAG CCATCCTGAG 1980
TTCAGCAGTG TGAATTGAGT GGTGGGAGTA AACACACACA CACGCATACA CACTCACACT 2040
CATAGATGCA CACCAGCTCT GGGCAACTTG GAGAGGACCT TAAATGCTCT GTCTCCCACT 2100
CTCCTTTCGG TGCCCTCCCT TGGGGTGATA TCACCAGACA CCATTCATTA TTGAGGCCAA 2160
ACCACAGCAT CCACCATCAT TATCCTCCTC CAGCCCAGAC GTAGTGCCCT CTTGCTCTCT 2220
TCCCTCCCAA ATCAGCTCTC AGCAGCACCT CTGGAGACCA TGTGTTGAAC TGTTTGTTAA 2280
GATGTGGCTG GGCATGCCAT TTCCACTCCT GTTTTGCTGT GTTTACAAAT AGGTTCTTAA 2340
GTCAGATCAA GTACATACCC CAGCCCAGCC CCTGTAACTG GTTCCATGGG TGTGAGGTAG 2400
GCCCTGAGAA TCTGTCTTTT GAACCAGCAC CCCAGGAGAT CCTAATACGG GAGGTTTCGA 2460
CAACTCTTTG GGACCCTAGC CTTTGCCTCT ATACACAGAC ATATACATTC TCTGCTCAAT 2520
CACAAATGTT GGCCAGGCAT 2540
|
