| Tag | Content |
|---|
EnhancerAtlas ID | HS129-03441 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:219046760-219049310 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr1:219047739-219047753 | ATGACTCACTTTCT | - | 6.49 | | Sox6 | MA0515.1 | chr1:219047280-219047290 | AAAACAATGG | - | 6.02 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I218873 | chr1 | 219046928 | 219048772 |
|
Enhancer Sequence | TCTTCTCCAA GTGGTGGCAT ATGGACTTGG GATCTTTCTA TCTGTGACTT TGCCTTTCTC 60
TAAGTCCTTG GGTTTTGTTT CGGGTTTTGG TTTTCTCTCC ATTCAGCTTG TTAGTGAGTA 120
AAGAGCATGT GCAGGCAGGG AGGATTGTGC TGAATATTTT AATAGGCCAG TTCAGGCAGT 180
GGCATGCATG ATGTCTACCA TTCACATTGA CCAAACTCAA TCACGTGGCC CACTTCAACT 240
GCAAGAGAGG CTGGGAAGTG TAGTCTACCT ATGTGCCCAG GATCAGAGGG AAAGGGTGTA 300
GCAGCTTTCC ATCATATTCA ATGGCAATAT AAAATGGTCT CCCAAATATA TTTGAACAAA 360
AAAGAAGAAA CAAATGTTTA TTGAATCCCA CTTCCAATAA TCTAACCTAA GCATCTCAGG 420
GATTATAAAG ATGAACACTC CTTCTGTGTT ACCCACAAAA GGCTGTGTAA TTTAATTGTA 480
AAAAGAAGAT ACTGTGTAGA TATTTGAAAA GTTGCAAATG AAAACAATGG GATATGCCAA 540
AGAGAAATAA ATAATTACCA AATAAATCAT ATAATCAGGC ATCACACATT CAAGGGAGGG 600
AAATTCACCA CAGTCTAAAG GGAGTTACAG AAGTTTCCAA AATGAGCAAA AGTTTTATGT 660
GGGTTATGAA AAATATGTCA GAGTAGACCA GGAAACAAGG GCAAAAGAGA CTTTTTTTAG 720
GCAGAGAGAA ATCCATTATT AAAAATGAAT TTTTCCCTAT TTAAAATAAC TGCCTTTTTG 780
TCATTATCAG CACTCTTAGA AACAGCAAAT TTAAATAGGC TGAATAATTA TTTAGTAATC 840
AGCTATTAAA TAACTATAAT CAAAATGATA TTTATGTGGC TTAATGTAAA GTTTCTCTTT 900
CCAAATATGC TTGTGCATAT AGGCGCAGTC TCAACTGCTA AACAAAGAGT GGGCTCATTC 960
AAACTTTGAA CTCAAATCTA TGACTCACTT TCTGTGGTCT CAGTTTCCTG CTTTACACAA 1020
TAGAGGAATA AGATGTCAGG GCTGTCTAGG GGATCCAGAT AATTGTCAGT TGGCTAGGAG 1080
AGTTTCTACA TGTTTTATAT ACACAGAGAT GATTATATGA CGATCAGGAG GAAGGTTGAG 1140
CAACTAGCAA CAGAGTCAAG AAGTGGGAAT GTGAGATGAT TTGTCTTTTT ACACGCACAG 1200
AAATAACTTA TTTAAATTGC TATGCCTGTC ATTGGGTTCG GGCCTTTGGA TCTAGCAATC 1260
AAGCCTGGAA GATGGAGCCA GGCTTGTAGA GAACCATCAT GATTCACTTC TTGCAGACAG 1320
CCTTTGGCTA TATACGAAAT AGATTGATGA TGATTATAAT GTTAATAATA ATAATAATAA 1380
TTTGCGCTTA CTTAGTAGCT TTCATGCTAT ATTTTCAAAG ATGTTGTAAA CATTAACTAA 1440
TGAAGCCCTA CAGCAACTCA TAAGGTAGCT ATTACCTGTA TTGTGCAAAT AAATAACCAC 1500
GGCCAGCAAA GGTTAAATGG GAAGCCTGAA GTCATATAGT AATTCAAAGC CAGGGAAACA 1560
GAGATTGATT TCTAACCACA ATGTTGGCTC CTTGACGTCT AGACCACTGT CCTTTCCTTG 1620
GCAAAGGAAG CTAACAGTTT GTAGAGCAGA AAATGGGTTA TGAGGGAAAG AGCAGAAGTC 1680
TGAGGTTTAG GAGTATGCAC AGGAGCTGGG TTAGAATTTC CCAGAATCAG TAATCCAATA 1740
GGGACATACT TGAAACACTG TTCCGCCAGA GCTAGCTTCC TACACAGGCG CTCGGCCGCC 1800
CTCACGGAGT CTCACGGCAG TGATCCGGGG ACATGTTTGG CTTCTTTACC AGAATACAGG 1860
CAACTTACAG GTAGAAAAGA GGCTATTTCC TTGAATTCCT TAACATTTAA CACAGTGCCT 1920
GGCATATCCG AGATATAATA AATAGATATG ATGTAATAAA TACTTTTTGA ATAAATAAAT 1980
GAATATGTAA AACACTTTTG TAAACTTAGT CTGAGTATAG AAAAAAATCA CTGTAAAATG 2040
AAATAATTCC AAAAAGCGAT GAAATTACTG ACTGAATTGA AAGAAAAGGA ACCTTCATGT 2100
AGAAACCTGA AACATTAACG TTGGTGGAAA ATACTGGGCT TGAAAGACAG GCCAGCATTT 2160
GCTCTGACAA TTGGCTACTC TACTATCTTC AGTTTACTCA TTTGTAAAAG GTAAGTATAA 2220
TAACAATGCC AGCCTCAGAG AATTGTCACA AGAATCAGAT GCGACAGTAT GTGCAGATCA 2280
CCTATCATTA GATCACACCA AGTCCAAAAT ACATATTTGT GTTCTTTCCT CCTTTGAAAA 2340
GCAATCGTAT CTCTAAACCT TAATAGTTGT AAATGTTTAA AATTAATATT CTTGCTTCTA 2400
TGTAGAAAAA GCTATTTTCA TATGGACAAC GCTTTCTTAG CAAGGCAAAA GGAGGGAAAT 2460
ATTGAAACAG TTTTCTCCCT AATGCTATGT GAGAAAGAAA AGACTAAAGC ACAACTAGCA 2520
TTCCATTTAA GCTGCACCGT CTTAAGAAAC 2550
|
