| Tag | Content |
|---|
EnhancerAtlas ID | HS048-14392 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr16:57466470-57467390 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr16:57466480-57466491 | AAGCAATAAAA | + | 6.32 |
|
| | 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 |
| GH16I057431 | chr16 | 57465820 | 57467328 |
|
Enhancer Sequence | CACTGAGTCC AAGCAATAAA AGAAAAAACT CCATAAACAC AGTCAGAAAC TATTAATTAC 60
AAACATACAT AAATGCTTCC TGCTGTGTAG AAGAGAACAC ACTGGCCTGG GAGGCAGAAG 120
ATGTGGGTTC ACAGTCCAGC TCTACCCCTC TGAGAGGTCT GACCTTGGGC CAACCACTTG 180
CTGATAGTTA CAGAAGTCAC CATTTGCTAA GCTCTTGCTT TGCACCAGGC ACCATATTAA 240
GCACTTATAT ACATTATCTA ACTTAATTCT GCTGACAACC TTATGAGGTA ACTATCTGTC 300
ATCCTACTTT TACCGCTGAG GAAACAGGTT TAGACACTTA GGCTGGTTCC ACAGGCTGCA 360
AAGCCTGTCT GATGCTTTTA ACCTCCATTC CATATTGCTT CCTCCTCGAT ACCTTAGTTT 420
CCATTCTATA ACATGAAGTT AAATTGTACT TCCTATGTTA CTGCAGGTGT TTTGAGGATT 480
AAATGAGAAA TGTGTCAAAA CCTTCAAAAA TAGCAGAGCT TTAGCCTCAT GTAAACCTGC 540
TACATACAAG AAAATAGGCT CTAGAGCTGC TGGTGGCAAG GTAACACCAT CAGTGGCAGA 600
CAAACCTCAC ACTTCCTGGT TCTCTGTCTA GTCAGGAGAA TGCAAGGAAG AGGCAGAGAG 660
CTGAGGCTCG GATGCAGTGT GGGCAAATCC TCGCAGGCCC TTGGGGTAAG AGTACCCTCT 720
AGTGATCATT GTCACAGCTG GATGCTCATA CCTTCCACAA GGCCAACTGT TCTAAGCTAT 780
TCCTACCCAT TCTGGAACCA TGAATCGAAA GGTTAGATTC CAAAGGATTT CTTGAAGATT 840
TAGGTTAGAC AGTCAAAACC GTACAAGTGG GAATGTACCA GTAAATATCT GTTAATGTCT 900
GCATACCTCA CAGCTGGGTC 920
|
