| Tag | Content |
|---|
EnhancerAtlas ID | HS053-03145 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr1:182936990-182938800 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF7L2 | MA0523.1 | chr1:182937673-182937687 | TCTCTTTGATCTTA | - | 6.12 |
| | | 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 |
| GH01I182968 | chr1 | 182937414 | 182939483 |
| Enhancer Sequence | AATGCCTCAG ACTCCCAAGT AGCTGGGATT ACAGGCTCAC GCCACAACAC CTGGCTAATT 60
TTTGTATTTT TAGTAGAGAA GGGGTTTCAC CATGTTGGCC AGACTGGTCT CGAACTCTTG 120
GCCTTAAGCG ATCTGCCCAC CTCAGCCTCC CAAAGTTCTG GGATTACAGG TGTGAGCCAT 180
TGTGCCTGAC CCCTATTTGG TTTTGAGTCA TAGACCCAAA TTTACAGAGC ATGGACTTTC 240
ATGCACAGTC ACACTGAGTT TTTAACAAGA GTATGTTCTC TATCACTAAG AATTCCAAAT 300
CCTGTTTCTT TTGGAGTACT CTTTAACTTA GATTCATTTT ATGTTTTAAA AGTCTAAGCC 360
ATAAATGTGT TTTGCTGGTA ACATGTTTCA TAGGTCAATT CATTGGTTGC AGGTTTGGAA 420
GGCTCGCCAC ATGAAGGAAT TACTGCTGGA TGAGAGATGC TGGAGCTTTG GACTGACCAG 480
GGACTCTGGC CAGACCTAGG CTGGCCCAGG GACTTAAGGC CCAAGGGAAC ATAAATGAAC 540
AAGTGCTGTT CAAGGGAGCC ACTCACCCAT CTTTTTCTGT GGATTCGTTC CTGCTGGGAA 600
CATACCAAAC ACGAAGGAAA GGGGAAACTA TCTTCATTTT AGATAAAGAA CTGCACGACT 660
TAAACTTTAT TTCTCCATAC CATTCTCTTT GATCTTAGGG TGAGTAAGAG GGAAAAAATG 720
TGCTTGTAGA GAGGTGAGTG AGAAAAGTGG TCATATCTTT GCCTCATAAA TGCTGAAAAA 780
CTTGAATCAC TGAATAGTTT TAACTGGCTT TTGCCTGTTG AGATAATAAC AATCACCTTT 840
AGGCAGCTCA GGGAAGAATA TAGTTATGGG GAATTTTAAA ACTCCAGTCA AGGTCAGTTC 900
AAAGTAGGTT CCAATTTGTC TTATAAATGT AATTTATTTC ATCTTGCCAA CTTGAAAAGA 960
TATTTTTCCA AAGAGCTTAG AAATGGAGGG TAACTATGGA CTAGAAAAAA ATGGAACAGT 1020
CTGGGATAGA ATGATTTGGG ATGGGTTGAA GCTCCCCAGG CACAAAACAA TTAAGATTTC 1080
ATTACATTCA TCATCAGGTG CCTCTCCCCC AAGTAGCATT TAAAGCACTC CACAATCTGG 1140
TCCATGCTGC CTTTTCTAGC CTTGTATCCT ACTAACCTTT CCTTATCTCA TGCAAACACC 1200
TGATTCCTTT CATATCATTT CTTACCTCTG GGCTTTTTTC AAACTGCTCT ATTCCTGTTT 1260
GGAATGCCGT CTTTCCCTTC CTCCCTGCAA TATCTGCCCA TCAAATTTGC ACTATTTATT 1320
TAAGACATAG TTAAAACCTG ACAGACTCCA AAATGTCTCA CAAGGTTCTT GCAGAAAAGA 1380
ATCTCACCAT CCTTAATAGT TACATAATAT TTTGTGTGTA CCAATATTGT ACACTTATCA 1440
CCATCACTAT CTGTCCTGTA TTACAGTTTA TGTGTTTATC TTCCACATTT TCTTTCCAAT 1500
GCATTGAGTG CAAGGGTCAC ATCTCGTTCA TCTCTGAGCC TCCATCTATG TGCTTTGCAC 1560
ATATTCTATA GTTCATAGGT TCAGTATGTT CCCATTTGGT TGTAGTACTT ATTCATTACC 1620
CATGATAATA GCTCACTCTG ATTCAGTCAA GCACTGTTTT AAAAGCTCTG CATACATTGA 1680
CTCATTTAAA ACATGCAATG CAGGTTACCA TTATTATCTC CAGTTTACAG TTCAAGAAAC 1740
AGATTACGTA AATATGCCCA AGGTTACACA GATAATAAGG AGCAAAACTG GGACTTGAAT 1800
CCGGAAGATC 1810
|
| |
|
|
|
