| Tag | Content |
|---|
EnhancerAtlas ID | HS048-02573 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:161186130-161187770 |
SNPs | | Number: 3 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX1 | MA0002.2 | chr1:161187349-161187360 | TTCTGTGGTTT | + | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TCTCTATCTA TCTATCTATA TACACACACA CACACATACA CACACACACA CACACACACA 60
CACACACACA CATATATATA TATATATAGA GAGAGAGAGA GAGAGAGAGA TAACCCTTTA 120
GGAAGGTAGG ACTCTGTTCT TGTGCTTGGG AGTAAGGCAA GGATATAGCC AAGACAAACA 180
GACGGGATTG CTGTTTCTAT GGGTCATTGT TAATGCTCCA TTCTGTCAGC AGTTGATAAT 240
GAGGGTGGGC AGCATGAGAT CCCCAGTTCC AGAGACCTGA GCGTCAGCTG AGAAATAGAG 300
GCAGAAATGG GAAGGTCTCT GAAGCTCTAC AGCTCCAGCC ACTATCTAAG AATTCTCACT 360
CCTCGTTCAC TCTGTGTTGT CTGTGCTGGA TTGGTGTGTG TGTGTTGGTG GCAGCTGGGT 420
GTTGGGGAGG AGGAGGTCAG TAAACTTCAG GGAAACTGTG GAAATTGAAA GAGAATGACT 480
GGGGAGGAAT TCCAGCAGCC TAGCTGAGAA GGTGGGAGCA AGTATTAAGT TAGCCACTGG 540
TCTGCTGCCG TGGGATGAGG AGGGAGGAGG CCCGCTGAGG CACAAAGGAA AGCATGGGCT 600
TTAGAGGCAG AAAACCTGCA TTTGAGTTCC AGCTCTGTCA CTTAACTCTG TGGCTCTGAG 660
TGAGTTACTT AGCTTTTCCG AGCCTTGGTT TCGTCACCCA TAAAATGGCG ATGATGATGT 720
TTCCCTCACA GGGTAGTTTT AAGATTTGTG CAATATCGTG TGTGTGAAAG AGTGTTGCAG 780
AATAAAAAGT ACTTGACCGA TGTCAGCAAT TGACTGACGT TAGTCACATG TTCCCTACTG 840
GTCCTCTGAT ACGGGGTGAG AGCAGTCTCT GGAGCCCAGA CTTGATTTGA TTTTTTAAAT 900
TGCACAAAAC TTCCCCTCTC AGAGACCCAG AGAGTGAGTA ATAGGGCAGA GTAACAGGAG 960
CTGGAATCCA TATAGCTGTG GTCATTCCCC CAGCCTTGTG TTCAGGGCCA AAGGTATCTG 1020
TAAGGTCTGG GAAAAACAGA CACACTTTTT TTTTTTTTTT TTTTTTTTAC ATATTTAAGT 1080
GTCTTGTGGT GGGACAGAAA GCAACAAGGC TGAGGCTAGG AGATGACCAA TGATAGAGTA 1140
ATTGCCTTCT CTCCCTTCCC CAGCTCACAT CCTTCCTGTC CAGCCCTCAG CCACAGGTCA 1200
CAGGACTTAG TAGAGACACT TCTGTGGTTT CTTCACTGAA ATTTGCCACT ACCTCTCCCT 1260
CCCACTACCC ATCTTGGCTG AGGTTTTGGT TTCAGTCCAG TGGACTCAGA TGGGTCCCTT 1320
GAGGTGGATA AAGTGCTCAA TGGTGCCTGA AGAACCCACA GTGCTAAAAA GAAAAGGTTG 1380
GGGGCTGAGG GGGAAGGCCT CAATTATTAG TCCGTGTGAG TCCCATTTCA ATAGAACCCT 1440
CAAGCTTCCT ATCCTAGCCT GACCCTATGG TGTGGGAGGA GGGAAAGGTA AGGGCAGTGG 1500
AAGGCCAGAG AGAAACAGAA TTTCTTCCCT TAGACGGCTC CCCTCCAGGC CCTGTCCTAC 1560
CTCCCAGAGC CCCTTCCCTT CTCTCCTCTG AGTACCAGAT CCTCCCTGAT ACCCCCGACC 1620
CCATGGGCAT CCTCTATCCC 1640
|
