| Tag | Content |
|---|
EnhancerAtlas ID | HS010-00925 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr11:94886080-94887350 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr11:94886462-94886483 | GTAATGAAAGTGAAACTGCGT | - | 7 | | IRF8 | MA0652.1 | chr11:94886465-94886479 | ATGAAAGTGAAACT | + | 6.06 | | IRF9 | MA0653.1 | chr11:94886464-94886479 | AATGAAAGTGAAACT | + | 6.38 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_12833 | chr11:94886077-94886209 | CD34_fetal | | SE_36837 | chr11:94885982-94887101 | HMEC |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ATTTTAGGTT TGAGGTGTTC ATTAGAAAAA CAAGTGGAGA GATTGATTGG GCAGACACAC 60
AGGTCTGGAG AGGGCTGGGC TGGAGATAGA AATATGGGTT GCCATGATAC AGGCATGGGA 120
CTGAAAGCCC CATCAGTCCC TTGGAGAGAT CATCAGAGAG TGAGTAGAGA CATAGCAGGG 180
CGAAGCCCTG AGCCCCGGTT CCCCCAGCAT GTACCTGCAG TCTGTTTCCT CTTCTCAACT 240
ACAATTCCCA TGGTCTTGTC TTGTTCACAG AACCTGCTCA AGGAGCATCT ATTAAATGAA 300
GGAACCCAAC TTTCATCACA TGTAAAATAA ACATCATTAT AATCCTACCT CATAAGGTTG 360
TTGTCAGAAA AAGTTAAACG TCGTAATGAA AGTGAAACTG CGTTATGATT GGTAGATGCC 420
TGCTATATTT TAAAATGTAG GCTTCATTAT CTCATTCTGT ACAGCTTGTA TTACTTGATT 480
GTATCTTCAC AGTTTCTGAT GCATGCAAGG CAGACACTCT CGTTCTCACT TTATTGACGA 540
GGAAAGTAGG ATTGGTGAGA CAAAATAAGT CCCTGAAGCT GCATATCTAA TGGTAACACC 600
AGTGGCTGAC CTGTTTGAGC ACATCTGCGG CAGGCACTGT GTTAATGATT TTGCATGTGT 660
TATCTGGCAA CAACACAGCG AGGTGGGGGT TATTATCTTC ACTTGCACAT GAGGAAACTG 720
AAGCATAGAG AGGGTGGTTA ACTTAGCCAA GGTCCCATAG TGAGTGGTTG GAAGAGTCTG 780
GGCCATGAAG CAGACCTGCC CATCCTGATT CAATGTTCTT TTTGCAGCCT GATAGCTCCT 840
CTTCTTCATC CCCCTACTAG ACTCCTGCCA GGGCCAAGCC TCACCACTCC TTCCCTTGAC 900
ATTGGCAACA TTCCTCTCTC CTTAACGTTT CTCTCCTACC AAGCCTGCTT GCTGCAGGAT 960
ACAAGAGTTC AGTCACTCCT TGGGAACAAC CTGCAGGTCA AAACATTTTG GCTTATTGCT 1020
TCCCCTTTCT GGAAAGTCCT TTCCCTTCCT CTCTGCCTTA TGAACTCCTA TGTGTTCTTC 1080
CAAACCCTGG TGAACTCCTA TGTGGTTTTC CAAGTCCAAT TAATATGTCA CCTCTGTTGT 1140
GAAGCTTTCC CTGCTTGCAC CAGACAAGAG GCATGACTTA GATCATGTGA CACTTTGTTT 1200
ATAGGTCTAT CAAAACAAAC TGACAATTTC CTGTGGGTTT GACTGATGCC CCTGTAATAT 1260
TGTGATTTTT 1270
|
