| Tag | Content |
|---|
EnhancerAtlas ID | HS034-05229 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr11:60917080-60918320 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXC1 | MA0032.2 | chr11:60917234-60917245 | ATATTTACATA | - | 6.62 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_09422 | chr11:60916713-60918248 | CD14 | | SE_29266 | chr11:60916582-60922165 | Fetal_Intestine_Large | | SE_31646 | chr11:60913799-60921667 | Gastric | | SE_42023 | chr11:60916861-60917210 | LNCaP | | SE_42023 | chr11:60917258-60918987 | LNCaP | | SE_65694 | chr11:60912444-60919190 | Pancreatic_islets |
|
| | 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 |
| GH11I061148 | chr11 | 60915634 | 60921982 |
|
Enhancer Sequence | AAAGAGCTGA TCCTGGACGG AAGCAAAGGA TGTGGCTCCA AACAAGCTCC AAACCAATCT 60
AGACAAGAGT CCTCAAACAT AAGCATACAT AGGGGGAATG TACAATCTCT CATAGGGAAA 120
TTGCTTCATG AAGGAAACTG TCATCTTTAC ATAAATATTT ACATAACAAC TGAATGCTCC 180
TCAATCCACT GAAAAACTCC ATCTGACCCC CCTTTGTCCA GAGGCAGGGC CGTCAAGTGA 240
GAAGACTCAA GAATAATAAG CCCATTCACT GTGCCAAATG GTGGGAGGCA CCCAGAGTGG 300
CAGAAGACTT CAGGAAATTA AGCCACTCAG CCGGCTGGGA GGCTCTATCA GCACGCGGCA 360
GGCTGCAGAG CCCAGCACTC ACACCCTGCC CCCTAGGTCG CTGGCTTGGC TTTGCTGACC 420
CAGTCCGTCC CCTAAAGGGA CTCCTCCCGA ACCTGCTGAA CCTCCACACA CACCTGCATT 480
CCAGCATTCC TAGATCTCCA CTCCTCTCAC TCTTCAACCA GACTTTCCCC CCAGCTTCCG 540
TTTCTATCAG TGACTTCAGC TCCTGGCCCT GACTTCCAGG TCAGCTCAGA CATGTGGGTC 600
CCCCCCACCC CTGATGTCCA ATCACCAAGT TTTAGCTAGT CAGTGTTCCA AAGGCTCTCA 660
CACACACCCA TCCCTGCCCT ATGCAGGCTG CAAACTAGTC TTCCCATCTC CAGGGTCTCT 720
TTCTCACAAC CATCCCACCA GGCTCCCCGG ATGAATGTGT CCTATCATGC TGCTTCCCTA 780
AGGCTGGCTG TCTTGCCCCC CTCCTCCCCT CACCGCCCCC ACCTGTCAAT GGGTGGCGGC 840
GGGAGGGGTC AAGTAGCCTA ACCAGTCTGG ACAAGACACC TCCCTCCTCT GCCCATTTGC 900
CCAGTTTGGC CTAATCCTGT CACTTTCAAC CTTTTTCAAA GGAGTTTTGT TTTTTTTTTT 960
TCCAAACAGA ACATTTAATC CAAACCCTAC TGCACAGAAC ACTTCACAAC ACATATGCTC 1020
TGGGCAAACA GGTCGGGGGG AGCCCTGTTC TCACAGCTCA GTTTCCCCCT TGACCTAGAG 1080
TTGGCCCCTG AGACCACCGC CCTAACCCCC TACCCCGCTG CTCCCAACCC TCACCAGCCC 1140
CTCCCCTGGT CCCCTCCTCC ACTCCCTTTC AGCTGTGATG TCTTGCCAGC AGCGTAGAGT 1200
GTGGGGAGTC ATCAAACCAG GCCTTACCGC CTCCTGCCCA 1240
|
