| Tag | Content |
|---|
EnhancerAtlas ID | HS145-13123 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr2:113835470-113836520 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr2:113835969-113835981 | TGCTGTGATTTC | - | 6.22 | | Gfi1b | MA0483.1 | chr2:113835969-113835980 | TGCTGTGATTT | - | 6.62 | | TCF3 | MA0522.2 | chr2:113835575-113835585 | AGCAGGTGTT | - | 6.02 | | ZNF263 | MA0528.1 | chr2:113835913-113835934 | CCCTCCCCTTCTCCCTCCCTG | - | 6.03 | | ZNF263 | MA0528.1 | chr2:113835906-113835927 | ACCCCCTCCCTCCCCTTCTCC | - | 6.81 | | ZNF263 | MA0528.1 | chr2:113835909-113835930 | CCCTCCCTCCCCTTCTCCCTC | - | 7.19 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_26693 | chr2:113834343-113836231 | Esophagus | | SE_26693 | chr2:113836267-113839903 | Esophagus |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr2 | 113835950 | 113836479 | | chr2 | 113835949 | 113836406 | | chr2 | 113835577 | 113835744 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I113076 | chr2 | 113834552 | 113838205 |
|
Enhancer Sequence | TGGTACCAGG TAGAGACACC ATTGTAGCCT AGAGGTGGAG CTGGCAGGGA GGGCTGGGCA 60
GGGCTTCACA GAAGAAAGAG CATATAATCT GGGCCTCAGA GAAAAAGCAG GTGTTTTCCA 120
GGCAGAGAAC GCAGGGATGG GCATCCCAGG CAGAAAAACT GCTCAGGAAG GTGTGATGAT 180
GGAGAAGAGC TCCCAGCACA TCTGAGGTGA GTCATCAATG TGGCTGGGAC CCAGGGCTTG 240
GACTGAGGAG TGGCTGCAAA TTCACATGAG AAGATGGGTG GCTCCTGATT GCTAATGCCT 300
TGTGAAGGAG TTTTTATCTG GGAGGCCCCA AGGAATCATC CAGGTATTTC AGGCAGGACC 360
CAGATTTTAA TCCTGGGCCC CTCAGATCAG CACTGGGCCA ACACAGATGC TACTGGGTCC 420
TCAGCTCTTC TCAGCCACCC CCTCCCTCCC CTTCTCCCTC CCTGACTTCT GTTTAGCACT 480
GCCCCGGGGT CAGCTTCCAT GCTGTGATTT CACAGTCAGC CTGACCCCTG CTTCATCTTC 540
CCTGACCAGT TCATCACCTT CATGCATGTG TTGAAAGACA AACTTTGGCA TATTAAAATT 600
TTAAGGAGTT TATTTGAGCA GAGAATGATT CATGAATCAC AAGGTGCCAA ATTGCAAGTG 660
ATTCAGGGCT CCACCCAGGG GCTACCGGAA AACCATTTAT AAGTTGTTCA GGAAGCAAAA 720
GGAAGAAAAA AATTCATTGG TTAAGTGGAA AATCCTTAGT TGCAGGTTAG TCGGCGGTTC 780
CTGATTGGCT AAGCTTAAGT TTCGTTTTCT TAGTCAATGA CCATTCACTC TGGGTTGGGT 840
TTTAGTTTAC TTAGGCAGGA ACCCAACACG CTGGAGTCAT CTCAGCCTAA TACCTTCCCA 900
ATTAATTATT TTAACACATG GTAACTCATT TCTGCTGGCC CTTCCCTTGT GAACTGTGCC 960
CATGGACCAC CCAGGCAAAT GCAGGCCTCC TCCTACTTAC TAGTGGTGCT GTTCCAAGTT 1020
GAATCATGTT CTCTATATAA CTAAAAAAAA 1050
|
