| Tag | Content |
|---|
EnhancerAtlas ID | HS034-15872 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr2:8597000-8598220 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr2:8597451-8597471 | ACCCACCCCACCACCACCCC | + | 7.21 | | SP2 | MA0516.2 | chr2:8597564-8597581 | GAGGGGGCGGGGGTGGG | - | 6.24 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_18145 | chr2:8595049-8598901 | CD4p_CD25-_CD45ROp_Memory | | SE_18871 | chr2:8595369-8598793 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19148 | chr2:8593122-8599085 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20078 | chr2:8592472-8600178 | CD56 | | SE_22866 | chr2:8594928-8599195 | CD8_primiary | | SE_28240 | chr2:8595810-8599825 | Fetal_Intestine |
|
| | 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 |
| GH02I008455 | chr2 | 8595589 | 8599654 |
|
Enhancer Sequence | CCTCGTCCAC TGTGAGGCTG GGGGGACGCC TAGTCGCTAG CTTCCCCGGT CTGGGGCCGC 60
GCTGTCTGAA ACCTCTCCAG AGGGGAAACT GAGTTCTCTC AGCTGACGAG GTTTCCAAGA 120
ACCCCAGTCC CCAGGGCCCT AGAATGCTGG CTGTGGACCG ATGGGATTCT TAGACCCGGG 180
TCACCTGCGT CAACAGCCCT GGGCTGGGCG GAGGGCAGCC CCGCACCTGC ACCTGCCCGG 240
CCGCCTAGGG GGTTGGAGGT GGCTCCACCG GACTCCTGTC GGGGCGCAGC CCGGACGCGC 300
CCGGCGGGCG TGGAGGCCGC TCCCGGGCGG GGTAAACGGG CTGGGGCGCG GGGTTAAGGG 360
GCGGGGTGGG GCGGAGGCTG TCTCCCGCCG CGCCTGCCTC GGATGAGGGC AGCACCTGCT 420
GGGCCGCTGA ACGCCCTCCC CTCTCTCTAC TACCCACCCC ACCACCACCC CGAACACCGC 480
CGCGCCGGCT TCTGCGCTCC CTGGGCCCGA TGCGGGGGAC GAGACGTGGG TGCGGGAGTA 540
ATGGAAGGTG CAGGGGAGGT CGGCGAGGGG GCGGGGGTGG GTGCAGGGAG GGCTGAGCCC 600
GCTGTGCAGG TCTGCGCAGC AGCCAGGCCA CCCAATCTTT GTGTTTTTTT TACCAACTTT 660
ACTGAATACA TATTTAGGAG CATGCATACA TACATACATA CATACATACA TACATACATA 720
CATACATCTT TTTTTCAGCC TTTCAGGAAA CAGAAAGAAG TGTTGAGAAA TAAGTAAGGT 780
CTCCTTTACG TGCTGAAATT GATTAAATAA ATAACCGAAG AAGCGCCAGG GAGCATCCTG 840
AGCCCGGGTT TGCTAGCCTT CCTCCCCGCG GTGGGTGAAC CCATAAAGTG AAATAAAACA 900
TCCAGGCCGG AACCAGCGAA GGCGACGTGG AGAGATGCGA CTGCAAACAC AATCTGCCCC 960
CAGGAACACC TCCCCCCTCA GCTGGAGGTG TGGACAAACA GGAACCAGCG ATAGCATTCT 1020
TAAAAGGTTA GATAAGGAAG GCAGGTGCAG CCTACCTGGT ATTTATCTTC TTGGCTTTTA 1080
CTTCCTAGAA ATATTTATCC TTTATTACCT ACTGTACTAT ATTTAGGACC TCATTGGGTT 1140
TCCGGCCGTT TTCTGTTTGG ACCGGTTTTT TTCTTGTTAC CTTGTTAATA TAAGCACGCA 1200
GGTTTAATTC CGTTTAAGAC 1220
|
