| Tag | Content |
|---|
EnhancerAtlas ID | HS145-12750 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr2:70161110-70162020 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata1 | MA0035.3 | chr2:70161684-70161695 | TCCTTATCTCT | + | 6.02 | | JUN(var.2) | MA0489.1 | chr2:70161649-70161663 | AAAAAATGACTCAG | + | 6.45 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_09668 | chr2:70157348-70164947 | CD14 | | SE_28042 | chr2:70158659-70163458 | Fetal_Intestine | | SE_28984 | chr2:70158659-70163479 | Fetal_Intestine_Large | | SE_65154 | chr2:70160227-70163073 | NHEK |
|
| | 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 |
| GH02I069931 | chr2 | 70158733 | 70163402 |
|
Enhancer Sequence | AGGTGCAAAG ATGCAGTAGA GATGGACTCT GTCCTCTAGA AGCTTAAAGT CTAGTTGAAT 60
AGATGACATA ATCCATTCAG CAAACACTTA TTAAGCATGT GTGTGTTTGA GGCACGGTGA 120
CAGCACAGCA ATGATTAAGC TGCAATCCTG ACTTTCTAAG GAGACTGCAA TGAATGGTTA 180
AGTAAGAAAT ATGAAACAAG TCAGGCAGTA CAGTGAACTT CCCAGTGAAT AATATAAACA 240
GTTAAGTGGT GCTTAGAAAA TAGAGGAATC ACTGTGAGCT AGGATGGCTT GGGAAGGCTT 300
TAAGGAGGTG GTAAGCTTAA GCAAAACCCC CAAATCTCAG CTGCTTCTTA CATTCATAGA 360
ATTTTCCAGG TTCTAGAATA AAGCACAAAC CATTTCAAGG AAATGTAAAT TTCTCAGTTG 420
GAGCAACTCT CGTGCTCTCT CTTCAGTCAG TTGCCGTGGC TGCTGCTTCA TCCAGCCCTT 480
CTCCCTCTCC CACTCCGTGC CATTGCATCA GTCTGACATA CTCCAAGAAC AAAAAGTATA 540
AAAAATGACT CAGTAAAAAC CCCCATCACT TCCTTCCTTA TCTCTGTCTG ACTGTTCCTT 600
GCCTTCTCCC TGCCCAGCCA GTTTCTTATG TGTCATTCCA GAGTTTGTCT ACATACAAGA 660
AAACATGAAT ATAGATTCTT GTTTTCCTCC ATCTTTAAGA TAGCATGGTA TACTCACAGT 720
TTGGAATCTT GCTTTTCTCC ACTTAACAAT ATATCTGGAA AATCTTTCCT AATAGGACAT 780
AAAGCACATT CTCATTCTTT TTGATAGCTA CATAGTACTA CACGGTGTGG ATGTAGCATA 840
ATTTATTTAA CCAGTTCCCT CCTGGGTGGT CATTTGGGTT GTTTCAATCT TTGCTATTAC 900
AAATAAAGCT 910
|
