| Tag | Content |
|---|
EnhancerAtlas ID | HS019-00947 |
Organism | Homo sapiens |
Tissue/cell | CD20+ |
Coordinate | chr1:117051090-117052190 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SREBF2 | MA0596.1 | chr1:117051248-117051258 | ATGGGGTGAT | + | 6.02 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_09543 | chr1:117049880-117054941 | CD14 | | SE_20393 | chr1:117051652-117052625 | CD56 | | SE_27848 | chr1:117050600-117052786 | Fetal_Intestine | | SE_28774 | chr1:117050433-117052792 | Fetal_Intestine_Large | | SE_39920 | chr1:117050416-117052476 | K562 | | SE_50584 | chr1:117050650-117052641 | Sigmoid_Colon | | SE_52493 | chr1:117050470-117052592 | Small_Intestine | | SE_57245 | chr1:117050708-117051515 | VACO_400 | | SE_57245 | chr1:117051799-117052521 | VACO_400 |
|
| | 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 |
| GH01I116507 | chr1 | 117050466 | 117053821 |
|
Enhancer Sequence | TGGCTTGGGT AGGGTAGACA GCATACTACA ATCCTGTCTT GGGAGCAGCA AGGCAGTGCT 60
GGGACAGGAC TATGACCCAG ATTCATATCT CCTAGTCACT GCTAGGTGAC TGTGGGCATG 120
TCGTCTCAAC TCAGTACATC TGTTCTCTTG TCTTCAAAAT GGGGTGATGC TATCTGATTC 180
ACCAAGATGT TTTGAGACTC AAATAAGATA AACATTTTTT AAAGTATTTG CCACAATGAC 240
AGGGCCATCA GAGTTGCTTT CATACCTACA CACCCTGTGT ACACTTGTAG CAATGAGATG 300
GAGTGAGGGA CTCCATTTCT ATGACAAGCA GCAAGGTTCC TGGGGAAGAG CCTACTCTTT 360
GGAGGTAGGC AGAGGAGATC TGGATACTGC TTTCACCAGC AGCCCATTGC ACATCCTTGG 420
GCAACTCACT TAATCTCACT GAATTTTAGT TGTGTCACCC AGGAATAATA GTAGGAAAAT 480
TCCATCTAGC TTGAGCTATT GTGGTGAGGA TTAAATAGAG GTTATGGGAT CAAAGGTGTC 540
TGGAACACAG GAGAGGTGGA ATAGATTTTA TCCTTGTAGG TATGACTCAG TCCACAAACT 600
AAGATCTGAA AAAAAATAAT GCCCTCTAGT TTCTATGACT CAACTTATTT CTGATTCTAA 660
GTTCCCATTT CTCTTGGTTG GTGAAGAATT TAAACCCCAC CCTTTTCTGG GGAGCCCGCT 720
GCCCTTGCAC TGTGGACTAT GACTTCACAT TATGAAGTAG GGTGGGGATT TGCCCTTGAT 780
CTTCAATCTA CACAGCTTAA GGCCAGATGT GCTTTGCCCT GTCTTCCTGT CCTGTGTCTC 840
TCTTGCTCCC AGGACATGTT CAAAGCACAC AATTATCCCC ACAGCTTGAG TTCAGAGGCA 900
GGAAACAAAT GAGTGCAAGA AAATAGGGAG GAGTAGAGCT TGTGAACTGC AGAGAGATGC 960
CCATCTAAAG GCATATCATT TTTTTTTTAA GTTTAATACT GTGAGAGCCA AAAAAAACAT 1020
GCCTGTGGGC TGACTGGGCA CATGAGCCTC TTCACTGGTC TGCGAATGTG CAGGGCCTGC 1080
TCTCACTTCA GGGCCTCTAC 1100
|
