| Tag | Content |
|---|
EnhancerAtlas ID | HS187-18280 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr4:6893150-6894490 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr4:6893260-6893281 | GGAGGAAGTGGGGGCAGGGGA | + | 6.07 | | ZNF263 | MA0528.1 | chr4:6893254-6893275 | GGAGCAGGAGGAAGTGGGGGC | + | 6.61 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_09487 | chr4:6891409-6896339 | CD14 | | SE_35384 | chr4:6893090-6897065 | HepG2 | | SE_50164 | chr4:6893265-6894973 | Sigmoid_Colon | | SE_52623 | chr4:6893286-6895668 | Small_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 |
| GH04I006891 | chr4 | 6893106 | 6896840 |
|
Enhancer Sequence | AACTCCCGAC CTCAGGTGAC CCGCCTGCCT CGGCCTCCCA AAGTGCTAGG ATTACAGGCA 60
TGAGCCACCG TGCCCAGCCT AAAGCAGGCA TGTCTTACGT GGCCGGAGCA GGAGGAAGTG 120
GGGGCAGGGG ATGTGCCACA CACTTTTCAA CAACCGGCTG GCACTAGAAC TCACTATTGC 180
AGAGATGGCA CCAAGCCACG AGGGATCCAC CTCCATGACC CAAACGCCTC CCATCAGGCC 240
CCACCTGCAA GATTGGGGAT TACAATTCAA CAAGAGATTT GGGCAGGAAC AAAATGTCCA 300
AACTCTATCA TAGTCCAAGG GTTGTGTTAC TAAGGTTTAC TTTCAGCTTG TTGACTAGGC 360
AGCAAGGAGT TCCATGGCCC AGTTTGAAAG TATTTAGAAG AATGAGGTAG TCACCGTAGC 420
CCCTCTCCAG GGTTAGGCCC CAAGCTGTTA CATACAGGGT TTGGAAACTT TTATTCAATA 480
ACATATATCA AGGACCTACT ACGTACTAGG CCCTAACCCT GATGCTGGTA ATACATTTTA 540
TTTTTCTGAA TCAGTCACCC TCCCTCAGCT CTAGTTCTCT GGCAATGATA GCATCACAAC 600
TTCCTCTTTA ACCTCTCCTA GATAAACTCC AGAGGGCCTC CCCAGCCTGC CTGCTGCACC 660
CTCTTTCTCC ACTTTTCAGG AGTTTGAGGG ATTTGGGCTG AAGCCCCACT CTCTGCATGA 720
GAAGATGTGT CATTATCTTG CCCCCAAATT CCCCAGCCTG GTGGCCCCCC AGGAGCCTCA 780
TGAAGTCAGC AGGCCGCTCC CGGCTCTGTC CTGACCAGCA GCGTGGGGCA GGGTGGGCAA 840
GGAGGGAGGC ACAGTCAGGG TTTATACACT CAGGGTGCAG CCCTTCCTGC AGAATAAGTG 900
ACGCGTTTCA TCTGGAGGAG ACACAGAAGG GTCCGTTTCC ACCCCATGAC TCTGCAGATG 960
CGCCACTGAC AGTGTGTGGT TTCCTTCTTG GCAGCGTCCA GCTCTCCGGC AAGTGGCTGC 1020
AGATCAAAGA AAGCAGCGGA AACCTCTAGG GGACACAGCC TCCCAGGGAC TGTGAAGCTG 1080
AACAGGGCGT GGCGGGAGGA GCCCTGGCTG ACAGAAATGC ACCCCCTCCC CTTTTCCAGG 1140
GTCAAGCCCC ACTCCCAGCC CTGTGGGAGG AGGGAGCAGG AAGAACCCAG TGTGTGGCGC 1200
CAGAGTGCCT GGCTCGAAAT TAATCCTGGT TCCCACTGTG TGGCCTTCGG CAGGTCATTC 1260
GCCCTCTGCA AGCCACCCTT TTCTCCTCTG TAAAACTGGA GTTTTAGCAC CCGGGACTGA 1320
GGGGCCTGGC ACACATGGGT 1340
|
