| Tag | Content |
|---|
EnhancerAtlas ID | HS170-02023 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr2:8443560-8444980 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr2:8443664-8443681 | CAGGACACCCTGACCTC | - | 6.03 | | ESR2 | MA0258.2 | chr2:8443665-8443680 | AGGACACCCTGACCT | - | 6.56 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_20349 | chr2:8440084-8447022 | CD56 |
|
| | 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 |
| GH02I008300 | chr2 | 8441085 | 8444444 |
|
Enhancer Sequence | AGTGAGTCAT TCATACCCAT CATGGTTATT TATACGGTAA TTTATATGGT CAAGCTTGAC 60
CGTCTTGGAG GGCTGCTGTC ATCACAAAGC AGAACAAGGC CCACCAGGAC ACCCTGACCT 120
CGTGCAGTGA GCCGGCCCTC AGGCTTGCAC AACAACAACC CCCAAACACT GGCATGTTCC 180
CAGCTGAGCC AACATGCACC AGACCCACCC AAACGTGGCC ACATCGGAGC CATCTAGAAA 240
CCGATTTGAA CACTGCTTCT TGTGGTGAGG GACAGGAAAC CAAGAGGACA CAGGGGGCCG 300
TGTCGAGGTT AACAGGGAGG GCTGCAAGCC CAGATCTCTG GTTTCTGTTC CTCTCCAGCG 360
TTCATCCTCT CCTACTGTTG TTAAAAATCA AATGTAAGAT GCAGAGAGCC AGTCCAGGCT 420
GTCCAGAGGA CAGGGCTGAG CCTCGCTCCC CACTCCATTC CCAGGGCCTA GCACAGGGCC 480
TGGCACAGAG GCCATATCAC AAGTCAAGAA GGAAATCTTT CCTTTCTGCC AACCCTGGAT 540
CTTCCCAGAG AGGAGCCCTG TGTCCTCTTG AGGGCAGGAT GGGTGGTCAA GGCAGGGACG 600
CGGTAAAAAC TAAGGTCGTA CACCAGCAAG CTATCGACAA GCATTTAGAA AGCTGTGTCT 660
CAACCAAGAT AGTTATTGCA GCTTTATTTG TGTTATCAAT AGTCAAAAAA AGGGGGGGGG 720
GAAGACAACT TACTCTGAGC CCTAGGGTGC CTTGTCATAG GAGGTTCTGG GGGTAGGTAC 780
ACAGTTACTA TTTATCCCAT GAATAAAAGG GTGGATGGAA ATAGGCCAGG AGTTGGGGAA 840
CTTCACACAA CAAAATCCAA ACTGAATGAT GGTGAGCCAA AACACAAAAA TAACACAAAA 900
GACCCCAAAT TGTTACTGTA TTTAGAAATA AGACCCAAAT TATTATAAAA AATTGTCAGA 960
TTGCTACAAG GCAATTTTTT GGGTGCTATA AAAGGCCTCT GGCCCAGGGG CCTAACAGCC 1020
TCCTAAAAGA GGATATCAGG AAAAGCAAGT CGCTAAATAG AAGAAAATAA AAGAAAAGGA 1080
ACTCGTCAGT CAAACTGCAT CCTGCCTAGC AGGGAATCCA CACACTCAGG GAATCTCAGA 1140
TCCCAGGACT TCAGACTGAG ATGGACTCGG TGTCTCTGGC CAATGAGAAC CAAAGTCCTT 1200
CACACATCAT GCTCCCTGAG ACAAGAAAAC GTAGGTATGC TTTAGGGGAA GAACAAAAAC 1260
AGACAAGGGC AGTGGGAGTT TTGATTAGCA TAATCTTTAC AAATCCTTGC TTTGGAATTC 1320
CAGCTTGGCC ACCTACTACA TCATTTGGGC AAGTTTCTTA ACCTCCCAGA ACCTCAGTGT 1380
CCTCATCTGT AAAATGGCAA TTATGAGAAC GCTACCTACT 1420
|
