| Tag | Content |
|---|
EnhancerAtlas ID | HS141-00156 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:12094440-12096080 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat6 | MA0520.1 | chr1:12094525-12094540 | GTTTCTCTGGAAAAA | - | 6.35 |
|
| | 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 |
| GH01I012034 | chr1 | 12094258 | 12094857 |
|
Enhancer Sequence | GCCTAACCCA GAGAGAAATG CTTCTTTTCC ATCACCGTAC AGGCTGGAAT GCTGCCACAG 60
GGCCCATAAT GCATCAGGGT GCATGGTTTC TCTGGAAAAA CAGTTCTTTT GAAACTTTGG 120
AAGACTTCCA GCTTGCTTGC TTCCAGTAAG TTCCATGCAC AAGAACCACA GCCCAAAGTC 180
TGTAGACACT GCGCTGAATG AAACCTGTGG CGCCATAGCC TGAAAGACCC TCTTTGTGTG 240
GCGGCAAATA ACTCCTGTCT TCCCACGTAC TGACCTCTGC TCTGCCTGTT CCTGGCTATC 300
TCTTCAGAAG GCAGCCTCCT TGGGGCCATC TGGAGCCATC AGCGGGGGTA GGAAGACCAC 360
AGCCTGAACC AGATCCTTCC TGCTGGTCGC TTGAGAACTC TTTTTCTTTT TAATTTTTGA 420
GACAGGGTCT GTCGCTTAGG CTAGAGTACA GTGGTGCAAT CTCGGCTCAC TGCAACGTCC 480
TTGCAAATTC AAGTGATTCT CATGCCTCAG CCTCCCGCGT AGCTGGGATT ACAGGCGCCT 540
GCCACCATGC CCGGCTAATT TTTGTATTTT TAATAGAGAA GGGGTTTCTC CATGTTGGCC 600
AGGCTGGTCT CAAACTCCTG GCCTCAAGTA ATCCACCTGC CTTGACTTCC CAAAGTGCTG 660
GGATTACAGG CATGAGCCAC TGCCCCTGGC CTCCGGAGAA CGGCAGGGAG GTGCTTGAGA 720
AAGCCCTGGG CCTGGGGCTG CCTCTCCAGT CACTTCTTAG GACTGATTTC AGCATGGGAT 780
ACAGGCTTAT TCAAGCTGAA GGGGCCCCAA GAATGAAGGT TCCAGGCAGG AGGCCCCTAG 840
AGCAGAGCCC ATGTCTTGCA GCTCTCCAGC ACCCACACAG TTCCATTTCG TGAATGTCCC 900
CACTACCCTC CCAGGTACTT GCAAGCTGTT CTTAATTCTC CTGGGCCTTT CACCCCTACA 960
ACTTGGGGTC ACCCTGGATG CTCGTCTTGT CTCCCACCCT TGCCCCATCC ATGTCTCAGC 1020
TTGGATGTCT CTTCTTTCAA GAGGTCCTCC CTGAACCTCT GGGTTCTCAG ATCTGCCCCC 1080
GCCATCACAC AGCCTGCCTT CCTGCTCTTC TCCAAGGCCC CTGAGTAGTA GTATTAAGTA 1140
ACTAACGGTG AGATGCATTG CCTAAGCTCT CTCCCCTGCG AGAATTGCAG CTTCCTGAAA 1200
ACAGAGATGG CATTGTTTTT CTTCATTGAA ATAGTTTTGT ATTGTACTTT TTCAAAAGTA 1260
CTGGCTGAAC TGTGTTCCAG AATTTGGCTT TTCCCTCTAG CCTGGTTTCT TACCTGCCTT 1320
GTGAAGGTTA CTGGACAAAT GCTTTCATTT CTCTGCATGA AAGGACCCTG GTGGTTGGGC 1380
ACACTCCTGA TACACCTTAC ATGCACCCCC TCTCCCATAC TGATAGCATT CTTTTCTTTT 1440
TTTGTGCCTT CTGAGTATGT ACTGTAAATC CCAAAGGAAA AAGGCAAGAT CACCTACTTC 1500
TCCCAAAACT AGTGTCTTGT GTTGGTCATT TAGAAATAAG AACAAAGATC TGACTCCTCC 1560
ATTGCCTGCA CCACGGCTTA GAACCATGAC CCTGGCCAGG CAGCGGCCTG AAGTTTGTCT 1620
TCTTGGACCT AACCATGCTG 1640
|
