| Tag | Content |
|---|
EnhancerAtlas ID | HS094-00626 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr1:31643200-31644700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr1:31643862-31643873 | GCAGGGTGTGG | - | 6.62 | | Klf1 | MA0493.1 | chr1:31643864-31643875 | AGGGTGTGGCC | - | 6.32 | | NFE2L1 | MA0089.2 | chr1:31643832-31643847 | ACTGCTGAGTCACTG | - | 6.71 |
|
| | 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 |
| GH01I031169 | chr1 | 31642701 | 31647752 |
|
Enhancer Sequence | TACAGGTGCA CCCCACTGAG CCTAGTGGAA TCTATATTTT ATTTTATTAT TATAAATTAT 60
TTTTGAGACA GAGTCTTGCT CTGTTGCCCA GGCTGGAGGG CAGTGGTGCG ATCTCAGCTC 120
ACTGCAACCT CCGCCTCCTG GGTCCAAGCA ATTATCATGC TTCAGCCTCC CCCATAGCTG 180
GGATTACATG TGTGGGCCAC CACGCTTGGC TAATGTTTGT ATTTTTAGTA GAGACGGGGT 240
TTTGCCACAT TGGCCAGGCT GGTCTTGAAC TCCTGGCCTT TAGTGATCCG CCGACCTCAG 300
CCTCCCAAAG TGTTGGTATT ACAGGCATGA GACACTGTGC CTAGCTGTAT CTGTATTTTA 360
GAAAGGCATC CCAAGTATAG TGAAGGTTGA GAAGCTCTAT CCCAGAATGT CAGCAGTAAA 420
GCAGCCAATG AGTATCATGC AAGCAAAGTC CAGCCCTCTC ATTTCACAGA TGACATCACC 480
AAGAGCAGAG TGAGAGTAGT TCCCCAAGGT CACAGGTTGT TGACAGAGAA AGAACTAGTG 540
CCAACAGTAG TGTCGGATAC CCAACACAAG GCTCCCTGGA GCTCCAGCTG GCCTGGGCCT 600
GCTCAGTCTC ATTCCAGGGC TGACTGAGGG GAACTGCTGA GTCACTGGAA CTGAGGCCCA 660
AGGCAGGGTG TGGCCTCCAT CGCCTGGTTA GGGGTGGGGC AGAGTGGGAC TGCCCCCACC 720
TCCTCTGGGT GACTGAGGCT GAGGCCGGAA GAGGGACAGG CAGAGAGCTC AGACTGCCTC 780
CCCATTCGTG GGACCCCCTC CCTTCACGTG AAACCACCTT TGCAAAGATT GTAACTGAGG 840
AAATTATGAC AGTGAAAGGG ATCTGACCTA ACCGACACCA TCTTGCTTTT AACCTCTAAG 900
CTGCCCTTGT TCATTCTTGG GTGTAGGCCA AAGTAACCTT GGGAAGGAAT TCAGTTTATA 960
CTTTAACTTT GAAACAAAAA TTATAATAGC CCTTTCCCGA AATAAACCCC CTTCTTTTTT 1020
TTTTCTGAGA CTGAGTCTTG CTCTGCTGCC CAGGCTGGAG TGCACTGGTG CGATCTCAGC 1080
TCACTGCAAG CTCTGCCTCC CGGGTTCACG CCATTCTCCT GCCTCAGCCT CCCCAGTAGC 1140
TGGGACTACA GGTGCCTGCC ACCACGTCCG GCTAAATTTT GTATTTTTTT AGTAGAGATG 1200
GGGTTTCACC GTGTTAGCCA GGATGGTCTC GATCTCCTGA CCTCGTGATC CACCCACCTT 1260
GGCCTCCCAA AGTGCTGGGA TTACAGGCGT GAGCCACTGC ACCCGGCTGA AATAAACCCC 1320
CTTCTTGCCT GGGGACCGGT CTGCCTTCAT AGGACTAAGA AATTATTGGC CGGGCACGGT 1380
GGCTCACGCC TGTAATCCCA GCACTTTGGG AGGCCGAGGC AGGCAGATCA CGAGGTCAGG 1440
AGATCAAGAC CATCCTGGCT AACACGGTGA AACCCCATCT CTACTAAAAA TACAAAAAAT 1500
|
