| Tag | Content |
|---|
EnhancerAtlas ID | HS141-01558 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:200865580-200866700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:200866205-200866226 | TGAGGAGGGAGAGGGGGTGGG | + | 7.32 |
|
| | Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
| SE_23181 | chr1:200859746-200868058 | Colon_Crypt_1 | | SE_24573 | chr1:200865700-200866870 | Colon_Crypt_2 | | SE_25202 | chr1:200865723-200866815 | Colon_Crypt_3 | | SE_27435 | chr1:200862320-200866901 | Esophagus | | SE_27875 | chr1:200859711-200868738 | Fetal_Intestine | | SE_28769 | chr1:200859522-200870222 | Fetal_Intestine_Large | | SE_33981 | chr1:200860158-200866875 | HCC1954 | | SE_50836 | chr1:200862222-200868005 | Sigmoid_Colon | | SE_52641 | chr1:200859983-200870293 | Small_Intestine | | SE_57019 | chr1:200865771-200866903 | VACO_400 | | SE_57734 | chr1:200865691-200866075 | VACO_503 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TAGTCATCCT AAGTATCCTG CGGGGTGGGG TTCCAGAATA TATGGCCAAT CTTTCAGAAC 60
TTTGGCATGT TTGCAAAGGC CTCCCATAAA GTTAAAAAAA ATAATTCTCC CATGCATTCT 120
CTAGACTTCC TTGAATAATT GAAATTCCAA AGTGCAAGGT ACATGTTGCT TTCAGGGCTT 180
TGTGTTTGAT TGTTGCTGCC TGTGGTTGCT GTGTTGTTTA TGTAGGTCTA TAAAAGTTCT 240
TGATCGTCCT GCTCTTATCA TCTTGATGGG TGGAGAGGTA TCACCAGGGA CCTGGCTGAC 300
AGCAGTCCCC TCTCCCTGTT GGCCTTGCTT TGTTACCAGC TTTCCCAAGG CCGACTTTTC 360
TGTCGTGTTG GCTGCCTGAG GAGGGGTGGA GCTCACCTCC CCCACCCTGC GGCCCCGCGC 420
TCTGAGGAGG CAGGATAGGC TCCAGACAGA AACTCGGAAG GACTTTTGGA CTCTTGCTCA 480
ATGGGCTGAC TCAGTGAGGA GGTGGCTGAG CTCTCTTTCC AGACCCAACC ACCTGCATGG 540
GCTCCGCCCA CCCCTCCCAC CCCTGCTGCA GCCAGCAGCT GCCAGGCCCT GGCCAGCTGG 600
GACCCCAACC AGGGGTGTGG GTTGGTGAGG AGGGAGAGGG GGTGGGCACA GGTGTTATCT 660
GGGTGACTGG TCCCTAGCTG AGCCGACACA ATGGGATGGC ACCTGTACCA CCCAAGTGTT 720
CTCCACCCCG AAGCAGGCAG AGGAGCAGGT GATCTCCTTT CTGTCCTTGC ACAGCTTCTG 780
CTCTAGTCAC TGCTTGCCCC TCTCCTGTCA ACTCTTGGCA ACCCTGATAG ACACAGCCCT 840
GGGTCTCCCC TGGCTGTGGG GTGTAGGGGA TCTAGGCTGA TTCCCCTTCA GTGGTCTCCC 900
AGGAGTAATT GATGGCTTGA AAGTTGTTTG AGGGCTTTGG GACAGCTCTC TGGCATACAG 960
TGGCTGCACA TATCTGCAGA TGATGTGAAG TTCAGAGTCC AGGGCGCCAA TTCAGAGAGT 1020
GGGCGTCCTG GACTTCGGAG GCCCCAGACC AGGGCCTTGG CCATGTGCCT GCCCACTTCT 1080
TGAAGTGTCC TCAGCCACTG GGGCGTAGGA CATGCCTCAC 1120
|
