| Tag | Content |
|---|
EnhancerAtlas ID | HS092-11348 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr12:13335300-13338000 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP2 | MA0593.1 | chr12:13337911-13337922 | TTTGTTTACAT | - | 6.14 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_26715 | chr12:13335657-13336747 | Esophagus | | SE_55863 | chr12:13335686-13337694 | u87 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I013182 | chr12 | 13335658 | 13337694 |
|
Enhancer Sequence | TATTACACAG TTTCAAGAAA AACAATTCTA TTGCCTACTT ATACCCTTTG GGTGGATACA 60
TCAGCACTTG GACTTTTCCC AGGGATGTCC GGCAGTCCCC ATCACAGCAT TGGGGACTGG 120
GAGGCAGCAC GAGGATTGCT TAGCAATGTC CACCGGGGAG GTAGCCTGGG TGGGAGGGCA 180
GTGGCTCTGC CCTCACCCAG GGGGACATGG GGTTGAGAGT TGCTCAGCCG CTTTCTAACC 240
TTGTGACCTG GTGTGCTAAT TTTCTCATCT GTTAGTTGAG AATATTACCT TATTATTATT 300
ACTTTTTACA GGGTTGTTAT TAGGCACACA TTAAGAGCTC AGCAAGTCAT ACCCATGATT 360
ACTGTTATCA TGATACCACA TAACTATGTG AAACAAAATG ACGAGCCGAC AATTGTGAAA 420
TCTGTCATAA GTCTGAAGGG TGCTAACATC AGTCAAACTT GTATTTCACT GTAGAACTGC 480
CAGCCTCGGG TCAATGACTA AATCAGGCAC AAAGAGAGGC TAAATAATGC ACCCCTGTCC 540
ACCACACTTG GGAGGTGTGG TTGGATGCAT GCTCTGACCT GGGGCACCAA GGTGGAGTAC 600
TTTGAGGGTT TGGGGCAAGT CCTGGGGAAG AAGAGTGGAG AAGAGGTGGG GAGGAGGCAG 660
GTGGGGCTGA CCAAGATGTA GGTCTGAATC TGGCATCAGC CTCCGGGCCA TGAACTCCTG 720
TGAACCTTCC TACCAGAAGG TGCTAGCTCA CCAGCATCAT AGGTTGTCCA TCCATCCTTC 780
CCTGGGGAGT GTCACTCAGG AGGGGACCTG GGGAGAGCTG GCACTGAGAC TTCTGCTTTC 840
CCATGCACTA TCTCTTTCCT TCTTATTGAT CTTGACAGTT CACCATGTGA GTGCTCAAAA 900
GCTTATGATA AAAAACCTGA TCAACCTGAT GGTGAAGCTG TAAGAAGTTT CAGGCATTTA 960
AAACTGGTCT GGATAAGACC TGGGGGAATC CTGTGGTCAG CGAGTTAAGA AGGATAGAAG 1020
GCCCTCGGAA GATTGAGAAA AGAAACATGG GGCTGCAGAG AGCCGAGTGT TTCGGAGCAA 1080
ATGAAAAGTC CATGGTGTGT GCTAGAGGCT CACACTCTGG GTGGCAGGAA GACCAGGTCC 1140
TGCTGCAAAT CTTACATCGG CTTCTTGAGT GTTTAAGTCA CTTTGCAATG TCATGCTCAT 1200
CACTGAGCTC TGGTCTCCCT TTGAGCACAA GGGACAAGCC AGGCTCTTCA CATGCACAAT 1260
TCTGTGTCCA TTGCTGATGA AGATTTCTCT TGACTTCCCA TAGGCTGAAT GGGCAGGCAT 1320
TCAAATACTT GATGATTCAT TGATCAACAA GGCAGTAACT AGGACTTTTT AACAATCTAT 1380
TTTTAAGGTT TATTGAACAC TTATTACATG CTAGGCACTG TGCTTTACAC ACATTATCTC 1440
ATCTTATAAA AACTTTATGA TACATGTACT CATATTTGTT TTGCAGGGAA GGAAATGAAG 1500
CCTCAGAGAG GTTATGTGAT ATGCCTCAGC CTCACAGTTA GTAAGAAGGA GGACTCCTGG 1560
GGTGGGGTTA CTCATTCTGC CTAGGGTGAG GTGGAAGGAT GAAATGGCCC CACAGAGGAG 1620
GTGACATTGA GACTGGCTCA CACCAATGGC TGTGAGCTTG AACACAGTGC AGTACTGCCT 1680
TAGCATCCAC CAGTGTTTAA TTTTTGACTT GTTTATGTCT ATCAAAGTAG GTTACCAAGG 1740
ATGGGTAGAT GTGTGATCTT TTGGGGCGAG TAGGATAAGG AGATAAACAT ATTTATAGTG 1800
CACTAATGTT ACAACCAATC CATTTTCACA ATCTTTCATT CATGTATAAA TCGATTTTGT 1860
TCAATAAAAA TAATAAAGCA CGCACTATGT TTAAGCATGG CTGGCCATTG GTGAGGGTTT 1920
AGAGACAAAA GATCATTCCT GCCTTCAGGA TCTTGCTGTC TCTTGGAAAC AGGGAGACAG 1980
AAAAGTGAAT ATTGGTAAAC TCAGGTGTAC TTAGAGGCTG TGGGAGCTCC CCGGAGGGGC 2040
ATCAGATTCA CACTAGGGCT GCGGGTGTCT TCCTGGGGAT GCTGGTGGCC AGGCTGAGTC 2100
TTGTAGACTA GGCCAGGCAA GGGAGAGCAG GCCAGGCAGA AGGGCATTTC ATCAGGCAGG 2160
ACATGGAATG CTTGGAGGTT TCAGGCTCAG GCACAGAGAG AGTTCAGTAT GGCTGGGACA 2220
AAAGGCAGGG AGAAGAGGGT GACAGGCTGG TGGGCCTGAG AGACAGGGAC AGTCAGACCA 2280
GGGAAGGCCT TGTGTGCTGG CCAAATAGTG GGTCCATATC CTAAAAGCAA TGGGGTGCCA 2340
TTGAATAGCT TGCTACAGAG GAAAGACTTA GTAGTTTTAG AAAACCACTC CGAGAGCAGG 2400
GGAGATCAAC CAGGACAGGG CAGCTGGAGA GGAGAGACAG GCTAGGAAGC AATGAGAGGA 2460
TCCAGGACAG TGAGCTAGAA GCAGGCTGCA GAGGGCTTGA TTGGGGGAGA CAGCTCTCGA 2520
CACTCACTTG CCCTCCATCT CAAATCAGAA AATACATAGA CTGCATTTGT TCTCATAGCA 2580
TTGTCATATT TAGTTCAAAC TAGTATCTCT ATTTGTTTAC ATCTAATGCC TATTGGTTAT 2640
AACAAACAGT CTACAAACAA CAGTATTGGG AGCCTCAGCG GCAGGTATTC TTCAAGGTCT 2700
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