| Tag | Content |
|---|
EnhancerAtlas ID | HS101-01265 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:40573140-40575550 |
Target genes | | Number: 16 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr1:40574335-40574347 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr1:40574339-40574351 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr1:40574343-40574355 | GTTTGTTTGTTT | + | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr1:40573880-40573895 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I040107 | chr1 | 40573024 | 40573835 |
|
Enhancer Sequence | GATACGTATC AAATTCTGAC AAAGACTCTC TCTTTGACCA AACTTTAGAC AGGCTCCTCT 60
GAGCCTTCTT TTCAACTGAA GGCAGGCCCT AATCTTTGGG TCTGTCCTCA GCCTGCATTA 120
CCCAGTTTTA GAGCAACCTT GCTAAGTCAG TTTAGAGAGA ATCCCCTCAT CCTTGAAATC 180
TGATCGCCAA CGATATTTGA TCATGATCCT CATTCCCCTC CATTGATATC TAAGTTCTTT 240
GCCTGCCTCT AGCAAGAATC CCGTTAGGCC GGTTTACCAA GAACCTCCCT ACCCTTGATG 300
TCTCCTCTTA ATAAATTTCT ATCCCCTGAC TCATCCAATC TACCTGTTGG CTATGAATCC 360
TTAGCTGTAT TTGCTGCATT AAGATTGAGC TCAGTTTTAC TGAACCTCTC TTCCCTATTA 420
CAATAGCACT GAATATTTGT CTTTACTACC TTTAACAAGT GTCTGGCTCT GTTTCTCTGC 480
AAGAATTCTA GGGTGCTATT CTTTTTCCCT TACAATTTTG AAGACTTTTT TTTTTTCGAG 540
ACGGAATTTT GCTCTTGTTG CCCAGACTAG AGTGCAGTGG CGCAATCTCA GCTCACTGCA 600
ACCTCTGCCT CCCGGGTTCA AGCGATTCTC CTGCCTCAGC CTCCTGAGTA GCTGGGATTA 660
CAGGAGTCCA CCACCATGCC CGGCTAATTT TTTGTATTTT TAGTAGAAAC AGAGTTTCAC 720
CATGTTGGCC AGGCTGGTCT TGAACTCCTG ACCTCAGGTG ATCCACCCAC CTTGGCCTCC 780
CAAAGTGCTG GGATTACAGG CATGAGCCAC CTCGCCCAGC CAATTTTGAA GACATTTGTT 840
GTATTTTTTT TTTTAGATGG AGTTTTGCTC TTGTTTCCCA GGCTGGAGTG TTATAGTGTG 900
ATCTCGGCTC ACTGCAACCT CCGCCTCCCG AGTTCAACCG ATTCTCCTGC CTCAGCCTCC 960
CGAGTAGCTG GGATTACTGG TGCATGCCAT CACGCCGGCT AATTTTTGTA TTTTTAGTAG 1020
AGACAGGGTT TCATCATATT GATCAGGCTG GTCTCGAATT CCTCACCTCA GGTTATCCGC 1080
CCACCTTGGC CTCCCAAAGT GCTGGGATTA CAGGCGTGAG CTGCCATGAC CAGCCAAACA 1140
TCTATTTTTA ATGATGATAA GTCTTATTGC TTTTTAGGGA ACCTATTTTG TTTTTGTTTG 1200
TTTGTTTGTT TGTTTCTCTT TGAATGTTTG GCTGCCCACT CAGATTCCTA TACAGAGAGA 1260
TGGCATGAAT TTCTTCTACA TGTGTATTTT TCCTCTAGGC CTATTCCTTA ATCATGGGCT 1320
CTATGCGAGC AGGAGAACCA CATGATCAGG GAGGCTTCTT TGTAGAATGC ATGGGTGGGG 1380
AGTAGTCAGG CAGTCTGATG ACCCCAAAAC TGACTCCATC ATGACGGTGA AGTGCATTAC 1440
ATGAATTACT CCTGAGTGAA GCTGCCACTT TTTTTTTTGT CCCATCCTTC TTTTTATGCA 1500
AGTCTGATCT ACTTTCTCTC AAGCTAAATG TTCTCTCAAG GAGTCCTCCC CCAGGCAAAC 1560
CACTACTTCT TTAGAGAGAC GTTCTCACAC TTCAGCGTTA GAGCAAAAGT TACCAGTACC 1620
AGATACCTTT ATAAAGGTGG AAGAATAAAA ACCCATTTGT ACCAATTGGT TTCTTAAATT 1680
GTTTTTAATG TAACGCTTGA ATAAATTACC TGATAGTTAA CTTAAATCTC ACTTTTGATT 1740
GTTTAAAATT TGTTGATTCT GAAAAGAACT GCCCATGTCC TCTAATCCTC ATCTCAAGCG 1800
TGATTTCTTT CCTAGATACC TACTCCTGTG TTCTCTCTTA CCCACTCTGT CCTCAACTTA 1860
TTCAGAGTAT CTGCACCCAT CTATTTACCT CGTTGTCTCA CCTTTAGACT AGCAAGTTCT 1920
CAAAAGCAGA GGCTAGGTCT AATTCACTTG GTGTTCAGAG GATCTCGCAC AAGGTTAGTG 1980
CCCGACAAGT TCCTATTTAA TAATTGAATG ATCACCAAAG GTAGACATTG CAAATACACA 2040
AATCCTTCAA AGGACAGCAG TTCCAGAATC TAGTCTGAGG AAAACATGGA AGGAGGATCT 2100
AGGGAGCCTG CAGTCTACCC ATCTGCAGCT ACTGAAGAAG CCCAGGCTGA AGCTCTGTAG 2160
CCTCTAGCAC AGGAAGAAAG TTGGGCATAG GCACTAGACA GGCTAAAGTT TAAAAAATGC 2220
AAATCACCAT CTTGGGCAAC ATAGTGAGGT CCTGTCTCTA TGAAAAAATA AAAATTAGCT 2280
GGACATGGTG GTACATGCCT GTAGTCCCAG CTACTCAGAA GGCTAAGGCA GGAGGATCGT 2340
TTGAGCCCCG GACTTTGAGG CTGCAGTGAG TGAGCTATAA TCATGCCACT GCACTCTGGC 2400
CTGGGGGACA 2410
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