| Tag | Content |
|---|
EnhancerAtlas ID | HS180-35776 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr4:6697100-6698610 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr5a2 | MA0505.1 | chr4:6698591-6698606 | GCTGACCTTGAGCCT | - | 6.9 | | Stat6 | MA0520.1 | chr4:6698282-6698297 | CATTTCCTGAGAACA | + | 7.08 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_32360 | chr4:6693831-6699251 | Gastric |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CTGGAATACA GACGCTTCCT CTCCCTTCCA GCCTTTTCCC CATATGAACA TTGCTGTGAG 60
TGAGATTTAC ATGCAATGTA ATTTCTTTTT GAGCTTAACA TTACAACATA AATTCTCAAA 120
CTCTGATGTT CATTAAACAC CCCAGCCCCA TCCTGGGAAC TTGGGCTTGG GGCTCGGGGT 180
GTTCTGATAA TGATCAAAGT ATGAGAATTG AACCCATGAG GACTTTGATC CAAGATACTG 240
GGGTGTGGGG AGGGGCAGGC ACAGGTGTCC TGGGAACACA CTTTGAGAAG CAATGGCAAA 300
GCTGGGGGTC CAGCTAATGT GTTACATTAG AATCACCTCG GGGAGGCCCT GGGTGCCCTT 360
CTCAGCCCTC CCTCCGGAGG CTGCTGAAGC CCAGCAAAGC CGGAGTCAGA GAACAATGTC 420
CGCCTGAGGG CAGGGCTGGG CTGGGCTGGC CTTCTGGCCC TATCTGCTCC GTGCCCAACC 480
CAGCGCCCCG CACAGTCGGA GCTTTGTAAA TACGAGGTGA CTGTCTGCCT ACAAACTTTG 540
TAAACATCAC TTGAAATGGC CGCAGGGTAT TGTGACATGG CCATACCACT ATTTGTTTGC 600
TATTGAATTT GTACTTCCCT GCCTTACTTT TGCTATTGCA AACCATGCTG TCACTAAGGT 660
CTTCATGCAC ACAGTTGTGT CTTGGTCAGA TGATATGTTT CTACCAATTT TAATTGTGTT 720
TCTTTCCACC TGGACACACA GCTCTCTGGC CCAGGGCTGG GTCATCAGCA CACCCTGCTG 780
CTGCTGTTCA GATCTGCATC CTGGTCCCGC TTGGTCCCAC AGTGAGAACG CTTTGCTATC 840
ACATGGGCAG GCTCTGAGAG CCCTGCCGGC CTGGCCTTCT CAAAGAAGAC CTGAGAGCTT 900
GGGACCCAAG CAGAGAGGAA GAACAGGGCT CAGGGTGCTT GCTCCATGCT CGCTCCACAC 960
CTGGGGCTCA ACCCTGGCTT TCCCCGGCTC CCTGTGTGAC TTCAGGGCAG GTCCCTTGGG 1020
CCCTCTGGGC CTTATCATCT TCATCTGTAA CAGGGCGATG CCTCTGCCGT GTCTGGTGGT 1080
GTTGAGGAGT TCCTGTTTGT GTAAGCAGCT AGTTCAGTGC CAGCACGAGA TGGGAGGCCC 1140
ATGAAGTTAG CAGTGCACAA AAAATAGAGC AAAGACTGGA TGCATTTCCT GAGAACAACC 1200
ATCACTGTAA AGCACTTTAC AAATCCAAAG ACAACCCCCG GCAAAAACTC AAAATGAAAC 1260
TCCCTCTCGC AGAGCACAAT TCCAATTCGC TCTAAAAACA TTACAAGTTA GTTCATGTCA 1320
TGCCAGATAG CTGAAGGCAG CTCACAAGTT CTTAAGGCCA GGAATGCCAT GTGTCTGCTA 1380
TGCACAGCTG GCCCTGGCCC TGACAGCAAA GGTGACGCAG ATGTGGGTGC CCTGCTCCTG 1440
CCCAGCAGCA GTGCTTGGTG GAGGCTGAGG CCCTGCACAG GCACCCTCAC TGCTGACCTT 1500
GAGCCTCTCT 1510
|
