| Tag | Content |
|---|
EnhancerAtlas ID | HS180-00077 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:2203270-2205160 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:2203545-2203560 | CGGGTCAAAAGGTCA | + | 7.44 | | RARA | MA0729.1 | chr1:2203545-2203563 | CGGGTCAAAAGGTCACTG | + | 6.66 | | ZNF263 | MA0528.1 | chr1:2204648-2204669 | TCTCCCGGCCCCTCCTCCTTC | - | 7.27 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_17322 | chr1:2202905-2205200 | CD4p_CD25-_CD45RAp_Naive | | SE_41586 | chr1:2201365-2203621 | LNCaP | | SE_41586 | chr1:2204609-2205679 | LNCaP | | SE_68719 | chr1:2201457-2203804 | H9 | | SE_68719 | chr1:2204755-2208710 | H9 |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH01I002270 | chr1 | 2201439 | 2203406 | | GH01I002272 | chr1 | 2203439 | 2204040 | | GH01I002273 | chr1 | 2204297 | 2211950 |
|
Enhancer Sequence | TGTGCGATGG CCCCAGAGGT TGACATCCTG GGGAGGATTG GCTGGTGATG CTTCCAGAAA 60
GTGGTTTTTG AAGATGCATC TGGTCCTGGC CCGTGGATGG CTGGCGGGAC TGGGAGAGAC 120
ACTCCGGGCC ACTGGCTGCT TTCTCGCAGC TGTTCTCCTC TGGGAGGACT TGCCCCTGTG 180
GGCAGGTGCA GGGGCACTGA GCGGAGGGGC TTGGGGGCCC CTGCCCGCCC CAGGCCACCT 240
TGCTCTCTCT CCAGGCCTGC GTCCTGCAAA GAGGCCGGGT CAAAAGGTCA CTGCCCCGAT 300
TTTTATTGCT GTCTCTTACG TTCTCACGAC CTCTTGCCCT CTGCACAGAT GGGCGGGGCT 360
GGAGCTTCCA CGAGGGCCGG CCTTTCCGGG GATTAAAAAC CCACTGAAAG GTCTGAGCCT 420
AGCTACCAAG CTTAAATGTC TTAGTAGCTT AAAAATGGTG TTAAAAATTA AGCAAAACAC 480
ACATAGACTT CCAGGTTTAG CATAAATAGA AACCAGAGGT GTTGAGACCG TGCTGCCCCC 540
TCAAACCAGC GCAGTGGAAA GAGGGGCAGA GCCCTCCACA GGAGCCCTCC GCTGGGGGGT 600
TGGGGAGACG GCCCTGGCCC AGCGTCTGCA GCTCCCAGCG GCACTGAATG GCAGTGGCCG 660
TCCCTGTGGT CTGGGGGCCT CCTTCCCCCA CAGGCTACAC AAGCCCTGGT CCTGCCAAGG 720
CTCGGGGAAG CCCTTTGTGA CTTTAGAAAA ATAATAATGG AGGGTGAACT GGTTCCTATT 780
TTTGCATTGT AATTGATTGC CAAGAACCCC TGAAATTAAA TACAACCATG TATTTTAAAT 840
GGTGTCCTTA ATGTAGAATG TTTTTATCAA AACCAAAACT CCCTGTTGAG GCCTTAGTGT 900
TCTGTCAATA GCGTGTTGGA GTCTGGTTCC CGTCTCCCCT GCCCCGGCCT ATGTGTGCTG 960
ACCCTGGGAC CGGTGAGGCA GTTCTCACCA CGCCCCGAGC CTCCCCCTCC CACGCCCCGA 1020
GCCTCGCCCT CCCACGCCCC TCCTGCCCCC GAGGCTCGCT GGCGTCTGTG CTTCTTCCAG 1080
GCGGAGGGGG AGGTGGTAGG CACCTTGGGT CTTAAATCAG AGAAACTGTC CCAGCAGTAG 1140
TAAAAGTCAT CAGCTGGCCC CAAAGAGCCC CTGGAAACAC AGGCTGTACC CCGCCTCCAT 1200
GGAGACATTT GGTGCCACCT GCGTTCAGTG CAGATGCCAC ACGGCTCTTC CTGAGATGGC 1260
TTCCGAGGCC ATTTGGCCCT TCATCTCGGG AACAGACCAA GGGGGTGTTT TCGGCCGTCT 1320
GAGACCCACC TGGGGGTGTC TGGGCCTTGG CCATGCTGCC TTCTCCAAGC CCCATGCTTC 1380
TCCCGGCCCC TCCTCCTTCC CACTGGCGCC GGAGACCTTT GGTAGTGGGT GTGGAAAGAC 1440
AGCAGCTGTG GGGTCCCTGT CCTGGCCGGC CACTCCTCCT TCCCGCCAGT GCCGGAGACC 1500
CTCGGAAGTG TATGTGGAAG GACAGCAGCT GTGGGGTCCC TATCCTGGTC AGAGGGTGGC 1560
ATTCCTCCCA CAGTCCTGGG AGCCACAGGG CTGAGATGGG ACTTCTCAGC TTGGCATGGG 1620
GAGGGCAGGA CGGGGTGGCT GCCATGCCTC ATTCTGTCTG TGATGGAAAC GGGAGGGCCT 1680
GGCCCTGCCT CTGTTACTGA GCTTGAGCCA GGGACACCCG TGACCCTGCC TGGGGCGGTC 1740
CTCCCCAGCC TTGTGAGCCA GGGCAGAGGT GCAGGTTGGG TGGCTGACCT GGTGGGGGGT 1800
AAGAACATCC ACGGAGAAGT GTGACGAGTG TGCGACCAGA GTGTGGACCC AGCCAGGAGG 1860
CCTGACCGTG ACTGCAGCCT CCCCCAGCAT 1890
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