| Tag | Content |
|---|
EnhancerAtlas ID | HS108-24299 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr2:219992620-219993930 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr2:219993359-219993370 | TCCTTTGTTTT | - | 6.32 | | Sox3 | MA0514.1 | chr2:219993360-219993370 | CCTTTGTTTT | + | 6.02 | | Stat6 | MA0520.1 | chr2:219992716-219992731 | AATTTCCTGAGAATT | + | 6.19 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27657 | chr2:219986089-219993383 | Fetal_Intestine | | SE_28744 | chr2:219985767-219993474 | Fetal_Intestine_Large |
|
| | 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 |
| GH02I219121 | chr2 | 219986199 | 219993382 |
|
Enhancer Sequence | ACTGGAAAAT AAACCTTTAG TCCAATCTTC TACCTCAGTG TCAGAGCTCT TTGGTATGAC 60
TTGGCAATTG AGATCAGATT GCTTTTTACT GCCTGAAATT TCCTGAGAAT TCCTTTTCCT 120
ACTCATCCCC ACTGAACAGG TTTAGAGCAA GACCTCTATA TCCATTAGGA AATAGCTCAA 180
CTCATCAGGT CTTAAGGTTC TAGAACAATG CTATTCAAAG TATGATCAGC AAACTGGTGA 240
GTGCTGGTCT GTGAACTCTT TGTAACTAGC CCATGATGCG GTAAGTATAG AAATTGAGTG 300
TAAGCATTTT AAAACTTTTA AAGCAACTTG ACATTACCAG GACATCAAAA CATGTATTCA 360
GAGGACTTAT CTCAATGAAC AGCGTATCAA ACAGTTTGAG TACTATTGAA CTTGTATGGT 420
AAGTCACATA TGGTACATGC TGCATACTAG TTAGGCACAT TAAGACCATA TGTCAGATTA 480
CTTTGAAAAG CACTATTCTA GAAAGTTTTC AGAAGGGAAG AGGATAGGTC TGGTGGTAGG 540
GGGGCTAGCT CTCTTCTTTT TTTCCCCCTT CTGGGTACAA TAGATAGTGA ATCTGCTACC 600
TCGGATGAGG AACAGGAAGC TGCTCCCACC AAGCCACTGA CTGCATGGGG TGAAGAGGAG 660
GGCAGGAGTT GGCGGCCAGG TTATCAGGCA ATAACAAACT CAGCATCCAA GCACGCGACT 720
TCCAGCAATG CAAGGAGCTT CCTTTGTTTT GGGAAAACAA GAGCTGCAAG AAGCCTCTCC 780
TTGACACGTT CTTGCCCGGC CTCAGGAGAA GCCCAACCAC CCCTGACACA CAAATAGGAG 840
AGTCCTGGCC AATGACCGGC CAGCCAGAAT CCTGACCACA ACCCCTGTTT GCTTTTCCTT 900
TTCCACCACT TCCTCAGTTC GAGGGCCACT GTGGGGCCAT AGGTAGCTGC CAGCCTAGGT 960
CACCCTTCAA GAACTTCACC CCCAATGACC CAGTACCTAG TCCATACAAC TCTTCCAATG 1020
CACTTCCTAT AGCCTACTTT CTATCCCCCA TATGGTTTGG TCTAAAAGCA AAGGCTTTTG 1080
GCCCCTTCCC TAGAGTTGTA GGTAAAATTA AGTCTTGGAA TACCACTCTA ACAAAGGCCA 1140
TGGTATGCTG TACCAAACTA AATCCAAGAA GATCATCATC TAACCAAGTG CCCAAGAAGA 1200
ACAATATTTG AGGCTTCAAT AGAATATTCT GAGCAACTAT TTTTACCTAA ACAGACTTAC 1260
TTGATTGCAT TAGATCCTCA ACTTCAAGAA TCCAGTTATC ATCAAGACTA 1310
|
