| Tag | Content |
|---|
EnhancerAtlas ID | HS040-00086 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:2177320-2178400 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr1:2177478-2177492 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_11007 | chr1:2177126-2179681 | CD20 | | SE_17322 | chr1:2177380-2179108 | CD4p_CD25-_CD45RAp_Naive | | SE_20071 | chr1:2177580-2178390 | CD56 | | SE_41586 | chr1:2177735-2178477 | LNCaP | | SE_46124 | chr1:2177298-2178497 | Osteoblasts | | SE_62490 | chr1:2120386-2191742 | Tonsil | | SE_68979 | chr1:2177579-2181412 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 2177405 | 2178400 | | chr1 | 2177615 | 2177829 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I002245 | chr1 | 2177240 | 2183861 |
|
Enhancer Sequence | CGCCTCCCAG GTTCAAGTGA TTCTCCTGCC TCAGCCTCCT GAGTAGCTGG GGCTATAGGT 60
GTGTGCCACC ACACCTGGCT AATTTTTGTT TTTTTAGTAG AGACGGGTTT CGCCACGTTG 120
GCCAGGCTGG TCTCTGACTC CTGGCCTCAA GCCGTCATCC CGCCTCGGCC TCCCAAAGTG 180
CTGGGATTAC AGGCGTGAGC CACCGCATTC AGCCCGTTTT TCTTTTTAAA GAACCGACTG 240
TTTTTCATAG TGGCTGCAGC ATTTTCCACT CCCAGCAACA GCGTTCGAGC AGCACTGTCT 300
TTGCATCCTC TCCAGCACTT GTTCTGTTTT TTGACAGCGG CCATCCTAAT GGGTGTGAGG 360
TGGCATCTCA TTGTGGTTTT GGTTCTCATT TCCCTGATGA TTAGTATGTT GGGCATTTTT 420
TCGTGTGCTT ATTGGCCACT CCTATATCCT CTTTGAGGAA TGTCTGAGTC CCTCTTTGAG 480
TCGAGTTGTG TGTGGGGGCC TTTGCTCAGT TGTACGTCTT TATCTACTCT GGTTAGTGAT 540
CCTGTTCTAC TTGTAAATTT CTGTCTCCTG TTTGTCTACT GCGTGCACCG TGGTCGGATC 600
CTGCCTCTGT TGCTGGAGGC TGCCTCTGTC CTCTGCTGTG GTGGTCAGGA AGCTGGAGCG 660
TCTCGGCGCC AGATTCATGT TTGTAAGAGG AGACGCTCTG TGAGCCTCGG TGTGCAGCGC 720
TGTCTGCAAG TCAGACTCCC CACCCCTCCT TTGTGCGAGC TGGGCGGGGG CTCTGCCGGG 780
ACTGGTGGTG TTCATGGAGA GGGCTTCTGT GTGATGAAGA GATGACAGTG ACCTGCTGGG 840
GCCGAAGGCT GTGAGTGCCA TTGGGGGAGG GAGTCTCAGA GAGTGCGGCA GTCGGGCCTG 900
ATGGGGCTGC TCTTCTGTGA AGGGGCACCT ACCGTGTGCC TGGCCTGTAG CAGCAGCAAA 960
GAGGAACCTG ATGGGGGGGG CCTCAGGAAC CTCCACCTCG CCCACTGTGG CCAGGCTGCT 1020
TCTGCTTTCT GGGAGGCCTG TGCAAGAGCC ATGGGCACAG GCCGGGCACG GTGGCTCACG 1080
|
