| Tag | Content |
|---|
EnhancerAtlas ID | HS180-04871 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:230843870-230845190 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:230843972-230843993 | TATTCTTCCTCCTCTTCCTCC | - | 6.98 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I230707 | chr1 | 230843691 | 230845900 |
|
Enhancer Sequence | GAGGCCAGCA AAGTTAGGAA GTGGGGCAGG GTCAGGGCAG CATGCGGTGG AGGCCGGCGA 60
GGATCCTGGG CTTCCTTTGA GTCCCGATGT GGTTGGCTTT TTTATTCTTC CTCCTCTTCC 120
TCCTGGCCTG GCTCTGCGGT CTGGGTCAGG TGGATGTGCT CTCTTTCGAA GGGAGACCCA 180
TTTCAGATGC CACTGGCTTT CTTGCCTTTG CCTTCTGCAG GACCCTCCTT CTCAGTGAGC 240
GCTCCTCCCA GCACTTCTCC TAGGGACAGC AGGCTAAGTC CATGTGTCCC TGCTCTGCCC 300
TGCACAGTGT GCTGCCACCC TCAACCGGGC AACCCTCGGG CTGGCCTCTG CCCCTGTGAC 360
CAGTCAGTGC CAGGGCTGAG CAATCCCCCC ATCTATCACC TCTCCCTGAA CCCGAAGGGA 420
AAGACCTCAA GGAGGTTGTT GTGGTAAGAA AAATCACTAT GCGCCACTGA ACCTCTTTCT 480
CCACAGTCTT GTCTTTCACC TCCCGCCTGG CTCTCTGTCC CTCACGAGGT TAACATCTTG 540
ACAGAGCCTC CTCAGTGTCT CTTAGACACA CCCCTCAGCC CCACCCCACC CATGGATTTG 600
CCGAGCTGCT CCCTGAGCAC GTGTTCCCGT GACTGTGTGC CTGGACTCTT GCGTAACCTT 660
CAAACAATCC TCCCTGCCTC CAGTCTGCAC ACGGCAGGCT TCCGGGATGA CCTCTGAACA 720
GAACGCGTCC CCATTCCCAC ACCTACCAAG CATGGCGTTC AAAGTGTCTC CAGCTCTGCC 780
CTCCCCAGGC CCATTTTCTG GTTCAACACT CATGCCAAGC CAACCGCCCC ATCCTCGTTC 840
CTTGCCCCAA ACTCTGCAGG CTGGGCTCAT CATGCTTGCT CCTAGCTTCA CCAGCCCTGT 900
TGCCCTCACT GCCAGGCAAG GCCTGCTCTC CGCTCCCCAG TGACCTCTGT CCTCTGAGAG 960
CCCCGAGGCT TCCCTGAGTT ACCTTGTGGA GCACGTTTCC CTGCAGCTCC AAATCCTAGG 1020
CATTTGCCCA TTGACCTTTA AAAGCCTGGA GGCAGGGCCT ATACAGCCCT CCTCTGGCCT 1080
CCTCTGAGAT GCCAGGCTTA AAGTCTTACA AGTAGCAAAT CCTCAACAAG TATTTGTTAA 1140
ATGAATGCTT TAAGCAATCT GTGGCTGGGT GCAGTGGCTC ACACCTTTAA TCCCAACACT 1200
TTGGAAGGCA GAGGTGGGAG GATCGCTTGA GGCCAGGAGT TCAAGGCTAC AGTGAGCAAT 1260
GATGGCACCA CTACACTGCA GCCTGGGTGA CAGAACAAGA CCCTGTCTCA ATAAAAAAAA 1320
|
