| Tag | Content |
|---|
EnhancerAtlas ID | HS187-03007 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr10:22780250-22781700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxa2 | MA0047.2 | chr10:22780902-22780914 | ACAAAGTAAACA | - | 6.18 | | ZNF263 | MA0528.1 | chr10:22781429-22781450 | GCCTCCTCCATCTCCTCCACC | - | 6.53 |
|
| | 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 |
| GH10I022492 | chr10 | 22780941 | 22781090 |
|
Enhancer Sequence | GAGGAAGATC ATACAAGGTT TCATGCTTGA GGAAGCATTT TCCCAACTCA AAATCTTCTG 60
TGTCTGCAAT CTACCATTGC TCTGGTTGCA AACCTGGCTT TGACCTTCAG CTCTGTAGTG 120
ACTTTTGGGT TGGTTCTCTG TACTTAAGTG GGACAGTTGT CCGACATTAG CTCATCTCTC 180
AATCACTACC TCTGACCTTT GTGCGTGCCC ATATCTACTT TGTCTCTTTG GTTTGCCCTG 240
ACACTCAGTT TGCAGAGATG CAGGCTTTTG TCTCTGGATC TTTATTCTCT GTCTCTGATC 300
TCATTACCCA CATGACTATG ATTGTCAAAC CTCCAGCTTC CAAGGGGCAG CATGCCAGCA 360
GACAGCCAGT GGGCTGAAAC AACATGCATG GGGCCAGTTG CTTGCTGACT ACAAGGCAGC 420
CAGAGTTTCA CAGGTGCTGT TGCATGGCAC CATTACAGAG GGCCAAAGAG GGATTTTCTA 480
GAGCCACGCT ATCTAGGTGC AGAGTTAAGG GGCTCATCTT ATTTCTTCAA GTTCTTTTGT 540
AAATTAGATG CTAGTTTTAT TTATTGATAA TACTTTTGCT TAAAAAGATG TTTTCTCTGA 600
ATATGAAAGT CAAACATTTT TATTATAGAT AATTTGGAAA ACATAAGGTG TTACAAAGTA 660
AACACATGAT CCCTGTCTTA CCATCTAGAC ATACTTAGCA AACCCTGCTA ATGCCTAGAT 720
CCTGTTTAGA TGCCGTGAGG TAGGAACCCT GTCTTGTGGT GTATGTGTCA CATAAGCCAC 780
AGGGACCACT TCCTTCCTAT TTAAGGTGAC TTCCACCTTC CCTCCTTCAT GCAACCCCAG 840
AACTGGGCAT TATCATCTCA CTACAGCAAT GCTTTCCAGC AGCCAATATG GTGCCAGGCT 900
TAGAGTAGCT TTCAGGCCCC TGCAACCTGT TTTGGAAGAA AGCTGTGTAT CAATCAAGAA 960
AGCAGCTGGC CTTGTGACAG AGATGGTTAG CTGCCTGCCA AAGCCTATCC TCTCCCTCCG 1020
TAGGACAGAC CTATAGCTAG GAAGCAGTGT GCAAACATAA GCTACATTGC CTGGCCCCCT 1080
TTGTAGTCAG GTACAAAGTC CTCATGTGAC TGGTCCTCAC AGAGACAATG TGAGCAGGTG 1140
TGTGGCATCT TGGGGTCAAG GCCTTTAAGA AGTAGGTGTG CCTCCTCCAT CTCCTCCACC 1200
AGCTTGCTGC AGATACTTAG GAGTAGAAGA TAATGGAGCT ACACATGAAA GGAACCTGGG 1260
TCCCTAGCTA TCACATTGGG GAAGGCCACC TTTGCAGCTA AGCACACCCA CCAGGGACCA 1320
CAACTTGAGC AAGAAATAAA TTCTAGAGTG TTGGCATCAC AATAAGTCTT GGGTCTATTT 1380
GTTACTGGAA CCTTGGCGAC CTTAACTAAT ATAGTCCTGC CAAATGCCTA GTGAATGCAT 1440
TAATAAATGA 1450
|
