| Tag | Content |
|---|
EnhancerAtlas ID | HS101-01341 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:43457290-43460030 |
Target genes | | Number: 28 | Name | Ensembl ID |
|
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 | chr1:43458317-43458329 | GGCAGTGATTTG | - | 6.04 | | GSC | MA0648.1 | chr1:43459351-43459361 | GCTAATCCCC | + | 6.02 | | IRF1 | MA0050.2 | chr1:43458926-43458947 | AAAAAAAAAAAGAAAGTAGGA | - | 6.62 | | SPI1 | MA0080.4 | chr1:43459727-43459741 | AACTTCTGCTTTTT | - | 6.27 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I042990 | chr1 | 43455998 | 43460310 |
|
Enhancer Sequence | CTGTGATTCT CCCCTGTGCA TGCTAATAAA TTTGTACGCC ATTTCTCCTA CTAATTTGCC 60
TTTTGTAAGT TGATTTTTTT TTTTTTAAAA GACAGAGTCT TGCTGTTGTC GCCCAGGCTG 120
GAGTGCAATG GCGCAATCTT GGCTCACTGC AACCTCCGCC TCCTGGGTTT AAATGATTCT 180
CCTGCCTCTG CCTCCCAAGT AGCTGAGATT ATAGGCGCCC GCCACCATGC CCAGCTAATT 240
TTTGTGTTTT CAGTAGAGAC GGGGTTTCTC CATGTTGGCC AGACTGGTCT CGAACTCCTG 300
ACCTCAGGTG ATTCACCCAC CTTGGCCTCC CAAAGTGCTG GGATTACAGG TGTGAGCCAC 360
CAAGTCCAGC CTGTAAATTG ATTTTTTAGT GAAACTTCAG AGAGTGAAGG GAAAGTTTTC 420
CCATAGCTCC TACACTGGGT AAAAGGAATT CCCGTAAAAT AGGCCTTTAG TCATGTGGTG 480
GAGGAGGTGT GGGGCAGGGG TGGCGTTCCA CAGTCCTGTG ATTAGCTCTC ACTCTTTTCA 540
TGAGCCTGGG AACCCTCCTG GGCTGTGAAG TTCACCAGTG CTTCTCCATT TTTTTCTCCC 600
CTTAGGTGGG ACAGAGATGG GAGTGGAATT GGCTATTTCC CCTCCCTCAG GTCAGCTAGG 660
CTCTGATAAA GCTCCAGAAG ATTGGGCTGG GCTAAAATAG TTTCTCTTGA GAAGCAGGCC 720
TTGTTAAGAA CAGAATGCTC TGGCATATTT CAAAATGGTT ACTTTTCCCA TCCCCCTGCT 780
GAAAGCACAA GGAGATTTTT CTCTGACATT CACTGGGAGG ACTCGATAGA GATCCTGAAG 840
ATTAAACTCA CAAACATGTG GGGACGCCCC TATGGCTGGC TCTTGCTGGA ATGTTTAATG 900
TTCAGATTTG CCCACGCTGA GCCTCCAGCT ATTCTTCAAT TACAGGTTAG GTTGTCCTGT 960
CCTGGTACCG GTTCTAGAGC AGGTTTCTAC TTGGGGGTTT CTCCTTCTCT GTCTCTTCAA 1020
TTTTGAGGGC AGTGATTTGC CCTGTGACCT GACTCCTCTA AAGGATCTAA GAAGAATTGT 1080
TGATTTTCCA GTTTGCTAAA CTTTTTACTT ATTATTAGGA CAGAGAGACA ACGTCCAAGC 1140
CCCTTACATG CCTGACTGGA CACTAGACGT CTCACTACCA TGTATTGAAC ACCCAGGTGG 1200
AAGTAAGCAC TTTTTACATA TTATCTCATT TAATCCTCAC ATTCACCCTG TGAAGTAATA 1260
CCACTACCCC ATGTTGTAGA GGTGATTCTT ATGGCTCAGC AAGAATTTAG TGACTCCCTC 1320
AAGGTCACAC AGTTAGAAAG TAGGATTTGA GCCGGGCGCG GTGGCTCATG CCTGTAATCC 1380
CAGCACTTTG GGAGACTGAG GCAGGCGGAT CACGAGGTCA GGAGATCAAG ACCATCCTGG 1440
CTAACGTGGT GAGACCCCGT CTCTACTAAA AATACAAAAA ATTAGCCAGG CGTGTTGGTG 1500
GGTGCCTGTA GTCCCAGCTA CTGGGGAGGC TGAGACAGGA TAATGGCGTG AACCCGGGAG 1560
GCAGAGCTTG CAGCGAGCTG AGATCACGCC ACTGCACTCC ATCCTGGGCG ATAGCGAGAC 1620
TCCGTCTCAA AAAAAAAAAA AAAAAAAGAA AGTAGGATTT GAACCTCAGT CTGTCTGTTA 1680
ACAAAGTCAG TGTGTGTCCC GCGCACCATG CCATGCCCCA GAACTAAGCA GATTCGGATT 1740
AGGTCTTCAG ACCCAGAGGC AGACAAAAGC CAGAAACAGA GACAGGAGCC CAGGCCAAAA 1800
TAGAGGATGG GACCCAGAGC CTCCGAAAGT TCCCAGGATG TATGTTTGAC AGACCATCCC 1860
CCAGGTCTCC AGAGGTAAGT GTTGAATCCC CCTTTTTCCC CTTTCCAGCT GCGTCACTTG 1920
GGTGAGCAGC TTTACCTCTT CTAGCCTCAA TTTTTTGGTA GGTAGCTCAG GGCCTGGCAA 1980
ATAGTAACTG CTCGAAAAAT GGAAGTTTGT CATTGTTGTT GCTAGGTAGT GGCTAATGTT 2040
ACCAGCTGGG AGGCCGTAAG TGCTAATCCC CTCCAGCTCT GGCCAGGTGA GGTCAGTAAC 2100
TGGAGATGAG GTCAGAGCCC TTAGAGGAAG GCACCCTGAC CCCAGCTGGG CTGGCTGGAG 2160
AGGTGGCAGC ATTGGAACCT CGGTGAAGAA GCATTCTGTT GACAGTTATA ATGAGATATG 2220
CCAGCTCTAG TTTCCCATGG GCACACCAGT TACCTCCTCT CCCTGGTAAC TGACCCAGTT 2280
GGCACCCAGT GCCTGAGAGC TTGACGGCAC AGTAGGATCA GTCTTTCTCT GGGGGCAGGT 2340
GTGCCAGCTG GTATAAAGGA AGAAAAGCCT CCCCGCTCCA GTGCAGAGCC AGCTCTGACA 2400
CTTCCTGACC AACTCCAATG CCAACTCTGA CACCGCAAAC TTCTGCTTTT TCAGAACGGA 2460
GTCACAGAGA CTAGATTTAC CCTCCCTTCT GAAATGCCTT AAAATACAAA ACCAAACAGA 2520
CAGACACACA CACACACAAA ATGGCACTCA AGACACTATC TATACATTAG ATAATGGCAA 2580
ACAGTGATCA ATGAGAGAAA CGAAGAAATA CAGGTTAGTC CTACTGACTT GTCACCTGGA 2640
GAAAATTCCC ATGCCATGGC TCCCCTCATT AACAAGACAT GTCCAGGGGC CTGGGGGAAG 2700
CCAAAGAGGC TGAAGTTTGT AAGGCAGAGC ACTGGAGAGA 2740
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