| Tag | Content |
|---|
EnhancerAtlas ID | HS082-10312 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr13:102143950-102146380 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| INSM1 | MA0155.1 | chr13:102144132-102144144 | CACCCCCTGACA | - | 6.22 | | IRF1 | MA0050.2 | chr13:102143958-102143979 | CATTGCTTTCTTTTTCTTTAT | + | 6.28 | | ZNF263 | MA0528.1 | chr13:102144115-102144136 | TCCTCCCCTTAGCCCTCCACC | - | 6.45 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I101492 | chr13 | 102144486 | 102146326 |
|
Enhancer Sequence | TGGATGAGCA TTGCTTTCTT TTTCTTTATT TTTTTTTAAA TTATACTTTA AGTGCTGGGA 60
TACATGAGCA GAATGTGCAG GTTTGTTACA TAGGTATACA CATGCCATGG TGGTTTGCTG 120
CACCCATTAA CTCGTCATCT GCGTTAGGTA TTTCTCCTAA TGCTATCCTC CCCTTAGCCC 180
TCCACCCCCT GACAGGGCCC CGGTGTGTGA TGTTCCCCTC CCTGGGTTCA TATGTTCTCA 240
TTGTTCAACT CCCACTTATG AGTGAGAACA TGCAGTGTTG GTGTTTGGAT TTCTGTTCCT 300
GGGTTAGTTT GCTGAGAATG GTGGTTTCCA CCTTCATCCA TGTCCCTGCA AAGGACATGA 360
ACTCATCCTT TTTTATGGCT GCATAGTATT CCATAGTGTA TATGTGCCAT ATTTTCTATA 420
TCCAGTCTAT CATTGATGGG CATTTGGGTT CGTTCCAAGT CTTTGCTATT GTGAATAGTG 480
CTGCAATAAA CATATGTGTG CATGTGTCTT TAAAGTAGAA TGATTTATAA TCCTTTGGGT 540
ATATTCCCAG TAATGAGATT GCTGGGTCAA ATGGTATTTC TGGTTCTTAG TTCAACCATT 600
GTGGAAGACA GCGTGGTGAT TCCTCAAGGA TATAGTGCAT CGCTTTCTTA CAGAGGTGTC 660
TGAAATAAAT GCAGTTCCTT CTTTTGAAAG TTCAAAGGCG TTAAGTCAAT ATATGACTGT 720
ATTTGTGGTC CTGCTCAGCA GTTATTCATT TAGGAGGTGA TTTGCTATTT TCTGAGAACA 780
GGGATATGAA ATGAATGTGG TTGCTTTTAG AGTCCAGAAA TCCATTTGGC TCAATGGAGC 840
TGACACAGTT TATTGCAGTT TTTAGGACCT TTTTGTAATT TACAGTGGAT ACTAATTTCC 900
TGCTCAAGTT TTCTTTGGCA GCTTCTGTAC AGCTGGAACA GAAGCTGGAG CTATGCCCTA 960
AGAGGGTGGT CTGGATTCAC TTCTGTGGGT CTACTCCTCT GCCTCTTCTT CTCTGTTCCC 1020
TCTTTCCTTT GCCTTTCTTT TCCCAAATTC CTCAAAGCTT GAAAGGGTGA GATTTTCCTT 1080
TTCTTTCCCT TGCTGCCCTC CTTGGAATTC CATTATGCAA TTCACCAGCC TCAGCTGTTG 1140
GTGGAATAAA TGGTAGCTAC CAGAGGAATT TAGACAATCC TTTCTCTTGG CTCTCAAGTA 1200
TATTGTCTCA CTGTACAATC CTCTTTTGAA TTCCCAAAGC CGAATATTAA CTCTTTCTTT 1260
CTTCGCATTG CTTCTGTAAT AATCCTAAAC TTCCTCACTC CCTTTCCTTT TCCAAGTTCA 1320
AATGCAGAAG CTTCAGGCTG CCTAAGGATA AAATGCGTTT ATGAAGAATT CCTTTACACA 1380
GAACTTTTCT GGGAGTAAAT CTCTGTTAAG CATGTAGTAG ATGTTGTACA AAGTTTATTG 1440
TGTAGATAAA TCCATGGGTT AATGGGTGGA AGGGGAGGTA GAAATTACAG ACTTTGTGGA 1500
ATGAGTAGAT TTCAAATCAT CCTTGGAATT TTCAAGATTT TACTCAAGGA GCTGATATTT 1560
AGAGCTTAGA TACACCTCTA CTATTTTATA AATAAAGGGC CAGCTGAACC GTATGAGTTT 1620
CTTACTTAGC AGAATTGGAG CTCTTGCTTT TTTGTCTTTC ATCCTCTATC CCAAAGATTT 1680
GTTGAAGGAT GATGAACTGA ATGAAGGCTG GGTATCTTTA AGAAGATACC AACAATGTCA 1740
CTTATTGAAA AAAAAAAAGC TATTTCGATT ACATAGTTTT AATAATCCTC ATGTCATGTA 1800
CTCTTATTAC GATTCTCAAT ATTGCAGTAA ATTGTGTTTT GTGGGGCTTT GATTAAAATT 1860
ACATTTTGCA CTCACTTTTA TGGTCTGGAG TGATTCTGAT CTATGGGGGG AGTGATAACA 1920
TCAGCATCAA GATTTTCTTT GTCCGGGACG TGCTTCAGCT GCATGACAAC TCTCCTCCTG 1980
AGTGATATGT GACTTGTGCC TTCATCACCT GTTCATCCTG CCAATATATT TTCCACATCT 2040
GTCCTCCCAT TCACCTAAAG ATTTATTCCA CATGCCTGAT GACAAAATGT CCTTGCACCT 2100
GGGGGACCTA AGCCTGTAGA ACATCTATCT CATTTTCTTT CTTTTGACAC AAGTCCATTA 2160
GCTTCATCTG TCTTGAGGAC AATCCCGGCT AAGAGCCTAT CTGATGTTTC TTCTTTGGGG 2220
ACCTTTCAGA ATTTCAAGGT TATAGGAAAC TTGGCTTTGT GCAAAGTATG TTGCCATCTG 2280
TTGCTAGTTT CTAATTTCAG ATCCATTTAA GAGATTTGCC AGGTTAGATT TATATAGACA 2340
TTTTAACTAA TTCTATTTCT TTGTACTTAA CCCAAGATCA CATACTTAGG TTTGTCCTTT 2400
CAATATCATT TATCAGAATA CTCCACTATT 2430
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