| Tag | Content |
|---|
EnhancerAtlas ID | HS180-04798 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:229073300-229074730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr1:229073867-229073878 | TTCTTATCTGT | + | 6.14 | | Gata1 | MA0035.3 | chr1:229073867-229073878 | TTCTTATCTGT | + | 6.62 |
|
| | 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 |
| GH01I228937 | chr1 | 229073150 | 229075248 |
|
Enhancer Sequence | GCCCTACGTT CTCAGGTGTG AACGGTGGAG TCAGGGGTGC TGAGGGTCAT GCTCACTCAC 60
CAACTACCCT GCACCAGCAC CCTCCCCCCT GCACTGGTTT TCTGTGCTCT CGTTTGGTGT 120
CCCCAAAATC TTGAGGCCTG TAGGATTATC ACCACTACAC AGAAGAGGAA ACCGAGGGTT 180
AGAGAGGTGG TCTGAATGTC TAAGAAGGGA GATCCAGGAT TGGAACCCAG ATTTGTACAA 240
CTCCAAAGCT CTCTTGTGAC CTGTGCCGCC TCCCAAGGGG TGAGCAATCG TGCCTCCCTT 300
TCCTCTGCTC AGCCACCCTG CAGCTCACAC AGCTGCAGTA ATGACTGCTC TCGAGAGAGC 360
TGCCCCACCC AGAGGGGTTT AAGGCAGAGA AGAGCGGCCT GCAGCCTAGT TTCTCTCAGT 420
GTGCCTTACA GCCAAAGCCA AAGACTGAGG CCGACTCCCA GGACAGGGCC GCTACCCTGG 480
CCTCAACACC ACAAATGACT GGACGCAGCT GCTGGCAGAA AAAGCCGCAC TCCAGGCATT 540
TAGTACCTAA CCGAAGAAAT CCAAAGATTC TTATCTGTGC CTTGCTTCTC AACTGCAGAG 600
GTTCTTCCCT TTTGTCCTAA CACACTGGGA GGGAACTCTG CACTGATGAC AAGTAACCAT 660
GAACGTGATT CCTTTCCCTC CTGCGGTGGT CATCTTCAGC AACTCTAGCC GTGAAGCCAG 720
CCTGCCTGTC TCTTTCTTTG CTTGTGTTGG GTCATATTAC TGAAGAAAGA ATAATAGCAA 780
CACTGTTACC CGCCTGTGTA CCAGTCTTTG TTCACGGGAG GTTTTAGGAT CTCTATGACA 840
CACGCAGGCA GAGCATGCCA CCGTCACTTA GGAGGGGAAG CCAGAGGTCT TGGAAGTCAC 900
ACACTAGCAG GGAAGAGACC TAGGTTTTCC CATGGCTCAC TGCAGCCTCC CTGAACTCTT 960
TTTCCACAGA TGCTAGGCTG ACACTCCCTT GTCCCCCTCT AGAGCTCTGT GAACAGGAAG 1020
AGGTTGTCTT CTAGCTGTGT AGAGGCTGGG GGAACAGCCC ACAGTGCAAG CCACGACTAC 1080
CTGCTCTGAA GTGGAGGGGC TGTGGAGCAG ACAGCAGACT TCTCCCAGCT GAGCAGAGCT 1140
GGGCAAAACA GATCGATCTA AACCGCCCTT AGCGGATGTT CTCATTTCCC TGCTGCCCTA 1200
AAAGTGGTGT CCGCCTGAGG TGAACACTAT AAATAACTGT TCACAGGCGG GTTGTTAAGG 1260
ACTCTATGGC CTGTGTTGGC AGAGACAGAT TCCGGGAAGT CAGTGACTTG GTCACTTCCT 1320
ACTTAAAACG CAGGGCACCA AGGAGCCTAT TTTGGGCTAA ATGCAAAAGC CTGGGAATCA 1380
AAGAAGAAAC GTTAGAGGAG AGACCGACCT CTTGCTTTTA GCCACAGTTT 1430
|
