| Tag | Content |
|---|
EnhancerAtlas ID | HS095-05939 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr11:94886050-94887280 |
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 | GTAGAGGGAT AAGACAGCTT AATGTTATAT ATTTTAGGTT TGAGGTGTTC ATTAGAAAAA 60
CAAGTGGAGA GATTGATTGG GCAGACACAC AGGTCTGGAG AGGGCTGGGC TGGAGATAGA 120
AATATGGGTT GCCATGATAC AGGCATGGGA CTGAAAGCCC CATCAGTCCC TTGGAGAGAT 180
CATCAGAGAG TGAGTAGAGA CATAGCAGGG CGAAGCCCTG AGCCCCGGTT CCCCCAGCAT 240
GTACCTGCAG TCTGTTTCCT CTTCTCAACT ACAATTCCCA TGGTCTTGTC TTGTTCACAG 300
AACCTGCTCA AGGAGCATCT ATTAAATGAA GGAACCCAAC TTTCATCACA TGTAAAATAA 360
ACATCATTAT AATCCTACCT CATAAGGTTG TTGTCAGAAA AAGTTAAACG TCGTAATGAA 420
AGTGAAACTG CGTTATGATT GGTAGATGCC TGCTATATTT TAAAATGTAG GCTTCATTAT 480
CTCATTCTGT ACAGCTTGTA TTACTTGATT GTATCTTCAC AGTTTCTGAT GCATGCAAGG 540
CAGACACTCT CGTTCTCACT TTATTGACGA GGAAAGTAGG ATTGGTGAGA CAAAATAAGT 600
CCCTGAAGCT GCATATCTAA TGGTAACACC AGTGGCTGAC CTGTTTGAGC ACATCTGCGG 660
CAGGCACTGT GTTAATGATT TTGCATGTGT TATCTGGCAA CAACACAGCG AGGTGGGGGT 720
TATTATCTTC ACTTGCACAT GAGGAAACTG AAGCATAGAG AGGGTGGTTA ACTTAGCCAA 780
GGTCCCATAG TGAGTGGTTG GAAGAGTCTG GGCCATGAAG CAGACCTGCC CATCCTGATT 840
CAATGTTCTT TTTGCAGCCT GATAGCTCCT CTTCTTCATC CCCCTACTAG ACTCCTGCCA 900
GGGCCAAGCC TCACCACTCC TTCCCTTGAC ATTGGCAACA TTCCTCTCTC CTTAACGTTT 960
CTCTCCTACC AAGCCTGCTT GCTGCAGGAT ACAAGAGTTC AGTCACTCCT TGGGAACAAC 1020
CTGCAGGTCA AAACATTTTG GCTTATTGCT TCCCCTTTCT GGAAAGTCCT TTCCCTTCCT 1080
CTCTGCCTTA TGAACTCCTA TGTGTTCTTC CAAACCCTGG TGAACTCCTA TGTGGTTTTC 1140
CAAGTCCAAT TAATATGTCA CCTCTGTTGT GAAGCTTTCC CTGCTTGCAC CAGACAAGAG 1200
GCATGACTTA GATCATGTGA CACTTTGTTT 1230
|
