| Tag | Content |
|---|
EnhancerAtlas ID | HS113-00642 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr1:27352830-27354530 |
Target genes | | Number: 26 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr1:27354351-27354361 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr1:27354351-27354361 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr1:27354351-27354361 | AATGGAAAAT | - | 6.02 | | SP1 | MA0079.4 | chr1:27353734-27353749 | TAAGCCACGCCCCAC | + | 6.16 | | SP4 | MA0685.1 | chr1:27353734-27353751 | TAAGCCACGCCCCACTC | + | 6.28 |
|
| | 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 |
| GH01I027026 | chr1 | 27353011 | 27355170 |
|
Enhancer Sequence | GAGTGCAGTG GCGTGATCTC TGCTCACTGC AACCTCCGTC TCAGATTCAA GTGATTCTGG 60
TGCCTCAGCC TCTGGCATAG CTGGGACTAC ACACGCAGGC CACCACGCCC AGCTAATTTT 120
TGTATTTTTT GGTAGAGATG TGGGTTTCTC CATGTTGGCC AGGCTGGTCT CAAACTCTTG 180
GCCTCAAGTG ATCCACCCGC CCCAGCCTCC CAAAGTGCTG GGATTACAGG TGTCAGCCAC 240
CATGTGCGGA CCTTCCCTTG CCTTCAAAGA CACCACAGTG TCCTAGTTTT CCTTCTGTTT 300
CACTGACTGC TGTGGTTTCC TCCGAATCCA CTCAGCCTCT AAAGAATAAA ATGCCCAGGA 360
CTTATTCCCT GGTCTTCTCT TTTCTGTCTA CACTCATTCC CTTGGTGATC TCACCAGTCT 420
CAAGCTTGAA ATACCATCTC TGTGCTGGCA AATCCCAGAT TTATTTATTA TTTATTTATT 480
TATTTATTTA TTTATTTATT TTTTGAGACG ACATCTCACT CACTCTGTCA CCCGGGCTGG 540
AGTACAGTGG TGTGATCTCG GTTCACTGCA ACCTCTCTCT CCCAAAATCC CAAATTTATA 600
TATTCCAGTC CAGAGCTCTG TCTGGGACTC CAGGCTCATT TATTTAATTT TAGTCAACAT 660
CTCTACTTTC ATGTTTGTAG TCATCTCAAA TTTTGCACGT TCAATGTTGA CTTCTCGAAC 720
TGAAGTCCTA GCAAATGGCA AATTCCAGTT CTTGGCCCCA AACTCTGAAG CCACTTTCCA 780
CTCCTTTTTC TCTCACGCTG CACTTTCTCA TTCGTCAGCA AGCCCTGTGG CTCTGCCTTC 840
AGAACCCAAA CAGGCCCTGA CCACATCTTG GCCCCACCTC CAGCTTACTG CCATCTCTGC 900
GGTCTAAGCC ACGCCCCACT CTCCAGGATT TTTGGAGCCT TTCTGCCGTC GTGCTTGTCG 960
CCTACAGTGT TTTCATCCCA GCAAGCCAGT GTGATCCTTT CTAAACACAA GTCAGATCAT 1020
GTCATTTTAA TGCCTCCTTC TCATTTGGAA TACAAGCCGA AATCTCCTCC CACACCCCTT 1080
CCCTTATCGG GGGCAGCCAC ACTGGCCTCC CTGATGTTCC TCAACCATGC CAGGCACGCT 1140
CCCACCTCAG GGCCTTGCGA CTGCTCTTCC ATCTGCCTGG CACGGTCTCC TTTGATCCCC 1200
ACATGGCTGC TCTCTCAATT CCTCCAGGTC GTCTTCTCCA TGTCTCCTGT TCTCAGGGAG 1260
GCCTTCTCTG ACTATCCAAT TAGAATGGCG CCCTCGCTCC CCACACCTGC TAGCCTCTTC 1320
TCTATTTCCA AAGCACCTAA CACCATCTAC CATGCTGCGT ATTTACCTAT TTATTGCCCC 1380
ATTTCCCGCC CCTGGAACCA AAGCTCCAGG AGAGCAGGGA TTTTGTTTTC TATGTAATCC 1440
AGCACCTGGA AACCTGTGTG TGCTCAGTAA ATATTCACGG GATGAGTGAA GGTGAGACAG 1500
GACTAACATG GGTCGCAGAA GAATGGAAAA TTCCAGGCAG CAGTTTCACA TGACTAGCAA 1560
AAGGAAGCTG TTGAAATAAC TGCAGAAGCT AGGGGCTCAT AAGACCCTGA ACAATCAGGG 1620
CATGGAGCAA GCTGGCTGAG ACCAACTGGA CACAGCATGG TGCTGGATTT GACCCAGGTT 1680
TCTCCTAGGA CCTCATTATA 1700
|
