Tag | Content |
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EnhancerAtlas ID | HS180-03791 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:180542930-180544250 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:180544183-180544201 | ACCTCCTTCCTTCCTTCC | - | 8.66 | EWSR1-FLI1 | MA0149.1 | chr1:180544187-180544205 | CCTTCCTTCCTTCCTTTC | - | 9.6 | Foxq1 | MA0040.1 | chr1:180543673-180543684 | AATAAACAATG | - | 6.02 | IRF1 | MA0050.2 | chr1:180544195-180544216 | CCTTCCTTTCTCTTTCTTTCT | + | 6.36 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 180543583 | 180543675 | chr1 | 180543231 | 180544105 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I180573 | chr1 | 180543045 | 180544340 |
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Enhancer Sequence | AGGTGCTTGG GAGGCTGAGG CAGAAGGATC GTTTGAACCC ACAAGGCGGA GGTTGCAGTG 60 AGCCGAGTTT GCACCATTGC ACTCCAGCCT GTGCAACAAA AGCAAAACTC CATCTCAAAA 120 AAAAAAAAAA AAAAGTCTAG GCTGAGCACA GTGGCTCATG CTTGTAATCC TAGCACTTTG 180 GGAGGCAAAG GTGGGAGAGC CACTGTGCCC AGTAGTTTGA GACCAGCCTG GGCAACATAG 240 TGAGACCCCC ATCTCTACAA AAAATATTTA AAAATTAATG GTGTGTGCCT GTAGTCTTAG 300 CTATGAGAGA GGATTGCTTG AGTCCAGGAG TTCAAGACTC CAGGGAGCCA TGATTGCACC 360 GATGCACTCC AGCTTGGGCA AGATAGAGTC TAAAGATAGA GTCTAAAGTC TTTGCCTCCT 420 CCTGGAAAAA TGTTATCATT GTTCTCTACC AGCGGAGTCT GTTTCTTTAC TCCTCCACTC 480 CTTCAATGAA TATTTGTTAA ACACAGCTCT GTGTTAATGC CTAATTGACA CATAAACATG 540 CAGAAACTAA GATATTTCAG CCATTATCAG AACCTTTTAA TCTTTTTGTT AGAGCCAAGG 600 AGATTCAGCT TTGTCTAAGG ATACGGTTAC AAATGAAGAA CAAGGAACAG AGCTGTATGT 660 GTATGTTCAA GGTTGCATGC TATTATTGTT CCTTCTAAAG CAAGGCAGAT ATAATCCTTG 720 TATTGGAAAC AGGTTTCAGG TACAATAAAC AATGTGCTCC CTTATCTCAG AAGCACAAAG 780 GTGGTTCAGC CAGTTGTTTA CCACTCAGGT ATTCCTTATT CAGCAGTTTT CGTACAAAAA 840 TGCTACCTTT TAATTTCCTA ATGCTCTGCC CTCCCAAAAG GTAATAAGAA ATAGAAACTG 900 GGTACTGCCT AAATGAATTC ACTTGTGTGG AAAACAAAGT CATTTTTATA TACTCCTGCA 960 ATGTGCATTT GACTACAAGC CAGAACATTT TACACAAGCA GTGGAATTCA TCTCTTGAAA 1020 TTGATTCAGG TTTTCTCTGA TAGGAGGGGT GGAAAAGGAA AATGAAAAGC ACGTGATTAT 1080 AATTGCACTT GGAAGCAGTC CCAGTTACAA GAGCAGTTCT TTAAAATTAT TCTTTTGGTT 1140 TCACCTTAAA TTATCTTAAT GGGAGAGTAC AGTTTAGTAG GAACAAGGAA AAGTGGGAAA 1200 AGGATACCTG GAAGTTTCTC TTTTCTCTTC TTTTGTCTTT TCTTTTCTTT TCTACCTCCT 1260 TCCTTCCTTC CTTTCTCTTT CTTTCTTTTC TTCTCTTTCT TTCTTTCTTT CTTTCTTTCT 1320
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