| Tag | Content |
|---|
EnhancerAtlas ID | HS012-12333 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr12:130095930-130098800 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr12:130097986-130097998 | TGCTGTGATTGG | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr12:130097299-130097314 | TGACCTTTTGCCCCT | - | 6.41 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I129613 | chr12 | 130098523 | 130100179 |
|
Enhancer Sequence | TCCACAGCTC TTGGCATTTT GAAAGGTTCT TCCTTTTGCT GTGATCCTCC TTGTCTACAA 60
CTGAAATGGG GGTTGTGGAT ATTTTTCCCA GTTACTTCCT TACTCATGGA AGCTTGGGGG 120
CCCAAGGCAT ATTTTAAGTG TAAGTAGCTT AGCACAACAA ACTTTTTCAC TTAGAAGTCC 180
AATGGACGTT GACTGGGGCT CTCCTCCATC CAGTGACTTA AGGATCCAGG CTCCCTCTAC 240
CTTGTAATGC CACCATCTCA ACACAGGGCT TCCAGGTTCA CTCCATCATG GGAGGACAGG 300
AATGGAGGAG GCACCCTGAT ACTGAAGTGC CTTGAACTAG AGATAATTCA TCATTGATGC 360
TCACATTTCC ATCCGCTACA ATGTCATCTT GTGGCCTCAG CCCAATTGTA GGGAAAGTCT 420
GGAGATGTAG GGGAGCACAG GGCTATTGGA TGAGCATAAA CCCTCAGCAA AGACTGTCTT 480
CCAGCCCCTT CCCACACATT GAGGAATACA CTTAACAGCT CCCATTCTGT TCCCACTAAG 540
AGAAACATCC CCAAGTCTCA TGCTCTCACT CCATCCAGCT CACAACGCAG ACACTGGGCC 600
GTGGCCGGTC GCAGTACCCT ATGGAGGTGT GGCTCTTCAT AGAAAGGAGA CAACTGATCT 660
CCACCCTAGA CCCAACATGC AATGGTGGAC CAAGGACAGA AGAAGGAAGA TGCACTCATT 720
TGCGAAAGGA GAGCTGGGGA GCACACAGCA GACCATGGGC TGTAACATCC ATCACATTTC 780
AATGACGGGC CCTGTAAGTT CTCCCTACAC TGAGCATGGG GGTGTCCTTG TTCACTGGCT 840
GATCTTACTA AGGGGAGGAA TTCCCTGTCC ATCACTGCCT GCGGCTCTTT TCTCTGCTCT 900
CCTGCAGCTC TGCCCTTTCC ATCCTCCCCC TTGTCAACAT CCACAGTGGG TGTAGAGGAA 960
GAAGGAACGC CTCCTGGCCA AGTTGCATAA ATTCTGCAGC CTGCTTCTTG CTCCTGGACG 1020
CTTGGGGGAC CAAGAATTGT TTCACATCTT AAGCAGTAAA AAAATAAAAA TAAAAAATCC 1080
TGTTAAAACT GGGCTAATGA TTTCTTCGAC AGGGCAATTT CCTTAAAAGT GTAGTAACGT 1140
AGTAGACTTA CTCTTACAGG CTTAAAGCTT AGTAACCTTA AAAACGTATT TGCTTCTGGT 1200
CTGTTCCATA ATCTATTAAT TATACCCAGA GTTCTTTTTA AAATATATAT ATATATATTT 1260
CTGAGACTCA TCTTATTTCT TTGTTTATCA GTCCCATACT GCTCCCCAAA ATGTGGGAAG 1320
ACATGTTGTT AATTTGGCCC CAGGCAACTC ATCTGATGTA CGCTTAGTCT GACCTTTTGC 1380
CCCTGAATCA AAGACCTGGG CTTTTTGGAA GGCAGAGGTT GCAGTGAGCC GAGATCACGC 1440
CACTGTACTC CAGCCTGGCG ACAGAGCGAG ACTCCGTCTC CAACAAACGG ACAAACAAAA 1500
AAAGACCTGG ACTTTTGTTG CCCAAAGGTT TTGTCAATCT AATATTTTAA CATTTCATGT 1560
CTAGACAAAG TCTGTTTTTC AACTTTGTAA GGCCCTGAAT TTCAGAAATC CCTCTATCCC 1620
TCATTTCCTC TTGCAAACAC AATTCCGTCC TGAGCCCATC TGTTCTATTT AATAACTTGC 1680
CAAACATAAA ATACTAACAT TCTGATATTA AACCTTTTTT CCTAGAACTA CGAGTTGGTT 1740
AGGCACAGGG TCCCAGTTGG TTAGACACAT TTCAGGAAAC AGCTCACCCC GTCACTTTGG 1800
CACGTAACTG CCAAGTCACT GCCTTGGTTT AGGTTTTTTT TTAGAAAGCA CCTGACTTCT 1860
ATTATCAATT TCTTAATTTG TCTGGTAATT TAACCTAAAT ATTATAAGAG ATAAACCCCG 1920
AATTCCTGCA TTGTAACAAA GGTCTCATGT AAGTTGATGG AGCCGCTCCT CTATCCACTG 1980
TCTCCTGGAT CTGCTCCATC CTCATGCAAA CAGAGAATGA CAGACACTCT CGTCTCAACA 2040
GGGCGTCTTC CCCATTTGCT GTGATTGGGG AAGATAAGAC TGGAGAAGGC ACACCCATTC 2100
TGTCGTGCCC AGGCCCAGCA GCAATATGTC ATTTTTGTTC ACATCGCTGC TTGACAGAAC 2160
TCAGTCACAT GACCCCAGTT TAAACTATGC AGGAGGCTGC AAATGTCAGG AAGCATACGG 2220
ATGTGGCTAG TGGGTGTGCC ATCGCAGCAA CTTCTAGGGA ATTGAAAAGT CAGCATCAGA 2280
ACCGAGAGGA CTGTCTCCAG CACCCAGAAG ACTGGCTCGA GAACCCAGGC AACTGTCTCC 2340
AGAACCCAGG GGACTGTCTC CAGAACCAAG GTGACTGTCT CCAGAACCAA GGTGACTGTC 2400
TCCAGAACCC AGAGGACTGT CTGCAGAACC CAGGGGACTG TCTGCAGAAC CCAGGGGATC 2460
GGCTCCAGAA CCCAACCAGC TCCAGAACCC AGGGGACTGT CTGCAGAACC CAGGAGACTG 2520
GCTCCAGAAC CCAGAGTACT GTCTGCAGAA TCCAGGCAAC TGTCTCCAGA ACGCAGGGGA 2580
CTGACTCCAG AACCCGGGGG ACTGGCTGTA GAACCCAGGC GACTGACTCC AGAACCCAGG 2640
TGACTGTCTC CATCACCTAG GCAACTATCT CCAGAACCCA AGGGACTGTC TCCAGGACCC 2700
AGGTGACTGT CTCCATAACC TAGGCGACTG TCTCCAGAAC CCAGGGTACT GTCTGGAGAA 2760
CCCAGGTGAC TATCTCCAGA ACCCAGGGGA CTGGCTCCAG AACCCATGCT CTTGAACCCT 2820
CTATCAGTGA GGACTGCACT TGTTGCAAAC AGCAGAAACC TAAGTAAAGT 2870
|
