| Tag | Content |
|---|
EnhancerAtlas ID | HS050-21532 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr14:93565020-93566420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr14:93565182-93565195 | GAAAATTCTGGAA | - | 6.14 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_05777 | chr14:93564824-93567869 | Brain_Hippocampus_Middle | | SE_07721 | chr14:93565399-93567804 | Brain_Inferior_Temporal_Lobe | | SE_09265 | chr14:93565231-93569171 | CD14 | | SE_28449 | chr14:93565112-93569308 | Fetal_Intestine | | SE_29311 | chr14:93564974-93569345 | Fetal_Intestine_Large | | SE_41563 | chr14:93565001-93566841 | LNCaP | | SE_48575 | chr14:93564915-93566001 | Right_Atrium | | SE_65267 | chr14:93564764-93567565 | Pancreatic_islets | | SE_68696 | chr14:93564995-93567792 | H9 |
|
| | 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 |
| GH14I093098 | chr14 | 93564895 | 93575036 |
|
Enhancer Sequence | GCAAAGCAGG GGTCTGAGCG CTGGTCCCAG CTTCTGCCAC CTTGTGCAGC ACCGAAAGGC 60
CCATGAAGCT ACTTCAGGGC TGTCCACACG GCCGCAACCA AGGCAGGGCA GAACGGCTTC 120
CCTTCCCGAG CTTCCCTCCA GCACTCCCAT GCAGCCGCCT CTGAAAATTC TGGAACACCA 180
AGCAGAGGCA CCCACAGCAG TTAAGCAGGC CCGGGGCAAG GGGCTCTGAG CAGGCCTTGC 240
CCTCACCTGC CCCACTCGTT TCAGAAAGGA ACCATAAGGG ACCCATACTC TAACCAGGGC 300
CTGTCACCCT GCACTTCTCC CAACCTCCAG CCCAGCCCCT TTGCCCGGGG CCCTCGGAAC 360
TGGGGCCCTG ATATATGGAA CATCCTGGGT TTGTGGCCAC CAGCCACTCA CCGTTCATTT 420
CCTCTCCCCT TCCGGGTGGA AATAGTCCAG CATGTCCTCC CCGCAGTTCC ACCAGGCCTG 480
CTCAGCTGTG GGGGGCCAGG GTCTGGCTTA GTATATCGGA GCGGAGTGTC CTGGACAGGA 540
GTGGCCCTCC CCAGACCAAC ACTCCCCTCC AGCTCCGACA ACCCCCAGCC ACTAGTTCAC 600
AGCTGCTCCA GGCTCTCAGA ATTCCCAGGA TCCAGCAAAA AGACACCTTC TCAACCCTCC 660
CCAAGCAGGA CAGGGTCAAA CAGCAACAGG CTAATTGTGT TTACATAACA CGAGATTGTT 720
TAGCTCCAGA ACACATCAGT GTCAAAACAC CAAGGTTCTG CACAGCGACA GCGACAGTGG 780
GGCAGGAAAG ATGTCATCCT TCTCCAGGAA CTCAGGCAGC ATTTCCCAAG GCCCGGAAAA 840
ACCCCAGCCC ACAAATAGGA CATCAGCCCT CCAGTATGTC CACCCACCCA GCTGGCTGCT 900
GGGCGCAGCC AGGACTCTCA GAATCTGCCT GTGTCGGGCT GGCCGTGGGA ATAAGCCAGA 960
TTCAGGTTTA ACTGAGGCAC AAGGTGGGGT CCAGGAAGCC GCTTCGGGGC TGCCCATGCA 1020
GCCACAGCCA CAGGGAGGCC CCGAGCAGCC TCCCTTCCGG AGCTTCCCAC CAGCACTCCC 1080
ACCCAGCTGC CTCCGAGAAT TCTGGAACCC CAAGCAGAGG TGCCCAGCAC AGGGTAGGCC 1140
AGCCTGGGGC TCAGACTTGT GGGGGTAGGT ACTCTCCACT CCCTTCTTGG GAACAACGTC 1200
CTAGCCCTGG ACTCTGTGTG CGAACCCTCA GGCCCCCGTC CAAGTCTTTG CAAGCTGGGT 1260
CCAGAGCTGG AAGCTGAGGG AGAGCAGCCC CCAGCCTCAC TCTGGCCAGC CACTGAAGCC 1320
CAGAAACAGG GAGCACGTCC ACTCCCACCT CAGCTGCCAA ACATCCCTCC CCTGCCTCTG 1380
GGAAACAGTG CCCCTGCAGC 1400
|
