| Tag | Content |
|---|
EnhancerAtlas ID | HS050-40393 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr2:234117440-234118980 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr2:234118220-234118240 | CCCCCCCCCACCCCCCCGCA | + | 6.73 | | ZNF740 | MA0753.2 | chr2:234118218-234118231 | GCCCCCCCCCCAC | + | 6.29 |
|
| | 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 |
| GH02I233208 | chr2 | 234117636 | 234119515 |
|
Enhancer Sequence | TCAAGCCCAA GGCCCCATGC CCACTTAGGA TGGATGTCTA GGCACTCCCC AGCATTTCTG 60
TGGGTTCCCA GGAGATACGG GTAGGAGAGC AACTGTTTGG GGCATACATC ATGCTCCCCG 120
TCACCTGCTC TGGGTTCCAG TCACTCAAGC AAATGCAGTG CCCCCACCAC AGTCAAACCC 180
AGGGCTGCTG TGAGGACCTG GCTTTGATTG CACGTGGTCG GACAGCTGAG GCCCACCTGG 240
TGCTCAGAAC AGGAAACGCT GTGGAATGCA AGAATTTTCA TCCTTGCCTT TTCCATCTCT 300
CTACCCTGCA CCCACCCCGA GAGGTCCCGG ACCACTTTCT CCCTAGGCTT TTTGCTGCCG 360
TGATCATCTG GGTTCCACCT TGACCAGGTC TCTCTCCTGT CTCTCCTTTC CTGACAATTC 420
TAGGCATTCC AAACACCCAG GTTCCCCCTT CTGGCAGAGG GGGAACCCAG ACATCCCCAC 480
CTCCTTATCA CCTACATAAT TCACCTCCAA GTAATTCACC TACACCAGGC TCCCTAATCA 540
AGAAGGCAGG TCAATTAGCC AGCTCTCATC AAAGTGCTCC ATTCCTAGGA TGAATTTCAC 600
CGCCCCCTGA GATTGCAGAT GCTGCTACAG TCACTGTTCC TTTTCAGAGG TAATTTTTTT 660
CCTTCTCTGC TTGATGCTAT GAAGGCTGGT TGAGAGCAGC AGAGTTTGTG CCGACAGGAA 720
GGTGTTACCC TCATGATGGA CAGTCTCTAG CAGCGCTCTT CCCAGTGCCT CCACCGCAGC 780
CCCCCCCCCA CCCCCCCGCA GCCTGGAGGG CAGCGCCTGC AGCCAGTGCC ACCTGCAGGG 840
ACAGAGTCAG CCACGGGCTC CTCCTCCTTC CTGCATTTCC ATTCTTTTTC CACACCATTT 900
TCCCCACCCG GATAGGAGAG AAATTAGTGA GTCATTCAGA AAAGCTCTCT CCCACAGCTA 960
CCTTCCCTGG TTCCAGCCTA CCAGGTTCTC ATCTTTGCAT GTCCTTAAAA TAGCTCCTTT 1020
CTCTTGGCAA ACAAATTTCC ATGGAGACCC AGCTATGGGA AGGCCCAGAA GCTTTCTGCA 1080
AGGCAGCAAA CTCAGCTCCC AGCCTTCACT CTGACAGAGA CCCTTTATAA TGCAAATGTG 1140
TGTTCTCACC CCCACAGACA CTGCCACCCA CGAAGGTCCC ATTTTGGGAA ATCTGAACCA 1200
CCCAGGGAAC GCACTGGGAG GTTGAGTCTA GGTATAGGCA ATCTAGTTTC TTGTTATTTT 1260
CTGACGGGCT GGCTGGCCTG CACTGGTGAG TTCTCTCTCA GGTCACAGCA GACCGAACCA 1320
CTAGGCTTAC CAGTGACTAA TCTCACAGCA GGCATACCCA GCTCATGCTC TTCCTCCATG 1380
CACTTGGCCA CACATGTTGA TGGCGTGCAC TGGGCCTTGG GGGTCAGTGC TTCTATTGAG 1440
GTAGGCCATG GGTGGGAGGG ATCCTGGACT ATGGGAACAG ATAGAATGGG GCTTAAATGT 1500
CTTTTATTTC CTAAAACTAT AATCTTGCAC AGGTTTCTTA 1540
|
