| Tag | Content |
|---|
EnhancerAtlas ID | HS113-02778 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr1:178119430-178121780 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr1:178120300-178120314 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | 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 |
| GH01I178152 | chr1 | 178121136 | 178121335 |
|
Enhancer Sequence | GTGATTCTCC CACCTTAGCC TCCCAAGTAG CTGAGATTAG CCCTCACGCC TGGCTAATTT 60
TTTTATTTTT AGTAGAGACA GGGTTTTGCC ATGTTGGGCA GGCTGGTCTC AAACTCCTGA 120
CCTCAGGTGA TCCACCCGCC TTGGCCTCCC AAAGTGCTGG TATTACAGGC GTGATCCACT 180
GCGCTCTTGG CCTGTTAGGT GTTTTTTAAA CCAAAATAAG AATCTACTGG TTTTCTCCAT 240
AGAAGATAAA ATGTTGTCTA TTGTTACATT GATGTGGACT TTAGGAATTT AATTCAAGTA 300
TTTCAATATA AAAATATTGA ACACTTCTAA AACCTGTGGC TTCTGTGGGA TTATCTGTTT 360
GTATATTCGT TGGATCCTCA TTATTCATCA TTATTCATGG ATTCTGTGTT TGCAAATTCA 420
CCTGCTTGTT AAATTTTATT TTTAACCCCC AAATCAATAC TTGTGTTGTT TTTGTGGCTA 480
CTTGCAGAGC AGCAAAAATT TGAGTCACCA GTCATTCATC TTCCCAGATG AGGTGGGAAA 540
AAAGCAACAC TCTGCCTTAT TATTTCAGCT GTTATACTGT AAATAAGCAT CCTTTTTGCT 600
ATTTAGTGCC ATGATTTTTT TCACTTCTTT TGTGCTTTTT CTTGGTGATA TGGTTGTTTA 660
AATGGTGCCA TATGAAGTGC TGAAGTGTTA TCTAGTGTTT GTAAGTGCAA GAAGGCTATG 720
CTCTACCTTC TGGAGAAAAT ATGAGTGTTG AATAAGCTTT ATTTAGACTG TTGACCATGA 780
GTTCAATGTT AATGAATCAA CAATATAAAA TAAGGTGCTT TAGCAGCCAG GCATGGTGGC 840
TCACGTCTGT AAGTAATCCC AGCACTTTGG GAGGCCGAGG CGGGTGGATC ACTTGAGGTC 900
AGGAGTTTGA GAACAACCTG GCCAACATGG TGAAACCCTG TCTCTACTAA AAATACAAAA 960
ATTAGCCAGA TGTGGTGGCA CATGCCTGTG GTCCTAGCTA CTCAGAGACT GAGTCAGGAG 1020
AATTGCTTGA ACCCAGTAAA CGGAGGTTGC AGTGAGCCGA GATCGCACCA CTTCACTCTA 1080
GCCTGCGCAA CAGAGTGAGA CTCTGTCTCA AAAATAAAAT AAAATAAAAT AAGGTACTTT 1140
AAACAGAAAC ACACATTAAA CAAGATTATG TATTGATCAG TTGATGAAAA TGTTGTGACC 1200
AGAGGCTTAC AGGAACCTAA CCTTGTATTT CTCATATTCG CTAAGCGGTT CAGTATTGGC 1260
TAATTCGGTG TTTGCAGTGA CATGGTAGAA CATAACTATT GATAATAACC AGAATTGATT 1320
GTATATTGTG GTAGCTCACC TCCAAAATGG CCTCCAATGA TCCAAGGCTC CTGGTGTTTA 1380
CATGCTAGTG TAGTCCCCTT CCACATTGAA TTATAGCTGG TTGACTCTGT GTCAGCAATA 1440
GAATACAGTG GATGGTGATG ATTTGTGCTT TCTGAGGCTG GGTCATGAGA AGAATTACAA 1500
ACTTCTGCCT TGATACTTGT GTTGTTCTTT CTGGAGGAAG CCAGCTGTTC CACTGTACCC 1560
AGAGGACGTC TGTATAGTCC TGTGGAAAGG CCCACCTGGA GAGGAACTTA ACATCCTGGC 1620
TGAGGTGTAG TAAATTTTAT GTTTGGTCTT TGTCTCTGTT CCTGGCACAG AGTTCCTTGA 1680
ACTCATGGAG TTTCCTGAGT GTTAGGAGAG TGTTTTGTTA GTCATAAGAA GTTCCTTTTG 1740
ATTACACCTA AATTTATGCT GGTGAGGTGA CTTAGAGTGG AGCCACTGAA TTGCCTCAGG 1800
ATATGGCTGG TAACCAGACA GACCATGTGA TTAGAGGGTG GAAATTTTCA GTTTCACTCA 1860
CCAACCTCTG GGGGAAGTAG AGGCTGGAGA TTGAGTCCTG TAGGAGCTCT TCCTTAAAAC 1920
AGCAGTGTTT GGTGAACTTC TGGATTGAAC ACGTGGAGGT ACTGGGAGGG TGGTTCACAT 1980
GGAGAGGGCA TGGGAACTAT GTGTCCCTCT TCCCCATCTT AACTTGCCCT ACGCATCTCT 2040
TTCATTTGAC TGTTCTTGGG TTGTATCTCT TATAATAAAT CGTAAATATA AGTACAGTGT 2100
TTTGTGAGTC ATTCTAGCAA ATTATTGAAT ATGAAGAGGT TGTTGTGGAG ACCCCTGATT 2160
TATAGCTGGT CAGTCAGAAG TATGGGTGGC CCCTCCAGGA CTTGAGACTG GTGCCTGGAA 2220
TTAGCCAAGC GTGGTGGCGG GCACCTGTAG TCCCAGCTAC TCGGGAGGCT GAGGCAGGAG 2280
AATCACTTGA GCCTGGGAGG CGGAGGTTGC AGTGAGCCGA GATTGGGCCA CTGCACTCTA 2340
GCCTGGCAAC 2350
|
