| Tag | Content |
|---|
EnhancerAtlas ID | HS180-03625 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:171312880-171314430 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr1:171313840-171313855 | TGGCCTTTGCTCTCC | - | 6.15 | | LHX6 | MA0658.1 | chr1:171314010-171314020 | ACTAATTAGC | + | 6.02 |
|
| | 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 |
| GH01I171343 | chr1 | 171312380 | 171314557 |
|
Enhancer Sequence | AAAAAAAAAA AAAAAAGAAG ACATAATAGT CCCATATTCC TTAGCATAAC ATAGAAGGCC 60
CTTCATGGTC TGAGTCCCTT TGCCTGGGTC AGCAGGATGC CTGTTATTTC AAACCCTCCC 120
ATCCAGCACT ACCAAACTAT GAACTTTCAT AACTCCTCCC TTTGGCATCA GCTCTTGCCT 180
CTGCCAGGCA CACAAATCTA TACCGTGCCT GACTGATGAG ATCCTATTTA TCTTTCAAGA 240
GAGCTCAGTG CTCTCATTCT GTGCAGCCTT CCCTAAATCC CCAAAGCAGA AATGGTCACC 300
CCTGTGTAGC AGCTGCACCT TGTGTATGCT CTGGTGCTGC TCTTTTCTTA CTATAGTATC 360
ATTTTCTTTT TGTCTGTCAC CTAACAAATG GTGAGTTCCT AAAAGGAATC ATATCATGTT 420
CATCGGACAC ACTGCCTGAT ATGAAGCATT GCTAAAGAAG TATTTGATGA ATCGACAGTG 480
GCCTTGCCAG CTGGCACTCT TTGTTTTCTC TCTTCTACCT ACATTCTTGT CTTCTGCCAA 540
CATGATAAAT TACCTCAGCC TTGCAAACAA ACAAGAACAG TCCGCCAACA GCTAATGTTA 600
TAAGTAAAGG ACAATCCAAG TGGCAATTAG AAGAAATAGA ACTATACAGT CCAGTACTTG 660
CACAGGAGCG AAGTACACTG GTTAAGAGCA CTAACTTGAG AATGAGAACT CAACTTGTTA 720
GCTATGAAGT CTTGGCCATG TGACTTAGCC TCTCTAAGCC TTAGTGTCCT CATCCGGAAA 780
ACAGTGGTCA TAATAGGGCC TACCTTACTG TGAACATTAA TGAGAAAATG CACGGTGTTT 840
GGTCCAAAGT AAGTTAACTA CTAATAGCTG CAGAATCGGG GACATTTTCT ATTCTCTGAA 900
TTAAAGAAAG GACTTGAAAC TATTGCCAAA TCCCATTCCC TGTTGTGTAA TCTGGAGGCA 960
TGGCCTTTGC TCTCCCTGGA TTCTCTGGCA GCACTTTCCA GTTAACGATC GTTTTTGTTG 1020
TTGCTGCTGC TACTGATAAA CGGACATGTT TAATGACACA TTGGTCTTCA CAGAGATGAC 1080
TACAGAGACT TTTAATCTAT AATCCAGTAG TATACAACCA TGCATCACAG ACTAATTAGC 1140
CAGATGTAAA ATAAACTAGC TTCTTACCAC AACTACCCTA TAAACATTGC AACTATTCTT 1200
TCCAAAATGA CCCTAGTCTT ACATGAAAAC ACCTATTGTG GGGAAACCGG AAACCTAGTT 1260
ATGTGACCAA AACTAAAAAT TAAAGGAAAA ATTGCAATTC ACTGGTGAAA GTTGGTGAAA 1320
GCAGAGGAAA TTCAGTGCCC TTCACTATGC TACTTTGATG TTACTTGTGT TCTTTTTGTC 1380
CCTCTTCTTC AGCCCATCCA TGTTAGTTCT CAGTAGGTTT GAATAAGCCA TCCGGAACTT 1440
ATTCACTTCT TTGGAGCTCA CCACAATGCT AACCTTCTTT TTCCCATCAG TAGTTCTTAA 1500
CAGACACCTG TCTGAAGACT CAAAGCCCGC AACAGAACCT TTCACTAGAA 1550
|
