| Tag | Content |
|---|
EnhancerAtlas ID | HS089-04114 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr14:35825940-35827100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr14:35826611-35826632 | GAAGGAGGTGATAAAGGGGGA | + | 6.01 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_23298 | chr14:35825743-35826271 | Colon_Crypt_1 | | SE_24327 | chr14:35825831-35826188 | Colon_Crypt_2 | | SE_27693 | chr14:35824207-35826830 | Fetal_Intestine | | SE_28626 | chr14:35824365-35826899 | Fetal_Intestine_Large | | SE_34130 | chr14:35825046-35826292 | HCC1954 | | SE_34831 | chr14:35824598-35826913 | HeLa | | SE_40331 | chr14:35825017-35826057 | K562 | | SE_50091 | chr14:35824854-35826224 | Sigmoid_Colon | | SE_52425 | chr14:35824985-35826233 | Small_Intestine |
|
| | 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 |
| GH14I035355 | chr14 | 35824234 | 35827035 |
|
Enhancer Sequence | CTCAAGCTCC CCACATGTCA TAGAGGAGTG AAAATCAGCC CAAACTTTTT GGAGAACAAT 60
TAGTCAGTAA TAACATGTCA AATGTGGATT CACTCTGATT CAAAAATTCT ATTTCTGGGA 120
ATCCACCCTC TGATGTTGTC ACACAAGGCA TATGCAAGGA TGTTCGCCAA GGTGTTGATT 180
ATCTAGTAAA ATGCTGGAAA CAACTTAGCT ATCAATTAGA GACTGGATAA ATAACTTACA 240
GTGTATCCAC ACTGTGGAAC CCTTAAGAGA CTGAGGTAGA TTTATATACA GTGACATGGA 300
AGATCTCTAA GACACATTGA CAAGTGAAAT TAACAAATCA AAATATGACA CATTAGTATA 360
ATTATATATA TATGTATATA TATTATATGT ATTTAAAGTC TCTCCCAAAT GCTAAGTCTA 420
TATCATTCAT AGAAACAGGT ATGGAGTCTG GGTGCAGTGG CTCATGCTTG TAATTCCAAC 480
ATTTTGGGAG GCTGAGGTGG GAGGATTGCT TGAGACCAGG AGTTCTAGAC CAGGTAGGGC 540
AATATAGCAA GACCCCATCT CTCTATTTCT AAAAAAATAA ATCCATGAAA CAATGTAAGA 600
AGAAAAAACA GGTCTGGAAG GAGATACACA CACAATGAAG AGTAGTTACC TCGAAGGGGA 660
AAGGAGAATT GGAAGGAGGT GATAAAGGGG GATTATAAAT TTTACTCCAT ATATTTCTGT 720
GTTGGATTTT TAATTTTATC TTATTTATTT ATTTTTCATT TCTTTGAGAC AAGATCTGAG 780
CTCTGTCACC CAGGCTGGAG TGTAGTGGCA TGATCATGGC TCACTGCAGC CTCAACCTCC 840
TGGGCTCAAG TGATCCTCCC ACCTCAGCCC CCGAGTAGCT GGAAGTACAG GCGCACACCA 900
CTATGCCTGG CTATTTTTAT TTTTTGTAGA GATGAAGTCT CACTATGTTG CCCAGGCTGG 960
TCTCGAACTC CTAGGCTCAA GGGATCCACC TGCCTCAGCC TCCCAAAGTG TTGGGATTAC 1020
AGGCGTGAGC CGCTGTGCCC AGTCTATCTT TGTTTTTAAA CAATGAATGT GCATTCATGC 1080
ATTACTTAGC GGCACTATGC ACGGTCATGG TGTTCCGTGT CGACCCTAGC TTCATTAGTT 1140
ACTAGGTGTG TAAGAAGTAA 1160
|
