| Tag | Content |
|---|
EnhancerAtlas ID | HS188-01997 |
Organism | Homo sapiens |
Tissue/cell | Th2 |
Coordinate | chr11:412620-414820 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr11:414397-414418 | CTCCTCTGCCCCTCCTCCCCT | - | 6.34 | | ZNF263 | MA0528.1 | chr11:413878-413899 | CCCTCTCCCCTCCCCACCTTC | - | 6.54 | | ZNF263 | MA0528.1 | chr11:414394-414415 | CCTCTCCTCTGCCCCTCCTCC | - | 6.89 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_23605 | chr11:414318-418165 | Colon_Crypt_1 | | SE_23968 | chr11:414308-415071 | Colon_Crypt_2 | | SE_24885 | chr11:412656-413134 | Colon_Crypt_3 | | SE_24885 | chr11:413237-413970 | Colon_Crypt_3 | | SE_24885 | chr11:414416-418679 | Colon_Crypt_3 | | SE_27233 | chr11:414457-418242 | Esophagus |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH11I000412 | chr11 | 412657 | 413134 | | GH11I000413 | chr11 | 413238 | 413970 |
|
Enhancer Sequence | CTGAACATGT CTGGATACAG TCGGGGAGGG GTGCTCAGCT CTGACCATGT CTGGATACAG 60
TCGGGGGGGG GGGGTGCCCA GCTCTAACCA TGTCTGGATG CAGTCGAGGG GGGGTGCCCA 120
GCTCTGGCCC ACGTCTGGTT ACAGTCAGGA GTGCACGTGA GCACAGACAC CTCGAAACAC 180
CTCGGGAAAC ACCTCGGGAA CCCTCAGCTT AGCCTCGCCC TGCGGTTGTG AGGCCGGAGG 240
GTGAACAGCG CCCGGTGGGG ATGGAGGTCT CGGGTCCCAT GTCCTTTCCC AGCCCGTAGC 300
AGCAGCCACA CACACCTCAA GTCTCCCAAA GCTCCTCAGT GAGGTGGCTG CAGGGAGAAG 360
CCCAGAGCCT CTTCCTTGGC AGCCCAGGGC CCCAGGGGCC TCTCCTCACT GGATGCCACA 420
GGGTCACCCT GTTTATCCAA CAGGCACTGA CTGTCTACTC CCCTCCCTGC TGCAGGGACA 480
CAGTGGAAGT GGGGATGTGG GGATCAAGCC TAAGTTTCTG CACCCCAGCT CCCTCAGGAT 540
TCCTCCCCGC TAAGGCCCCA GAGGCAGTGG CAGGGACAGT CCTCTTAGCC TGCCACCTAT 600
TCCCTCTCCA TGGGTGAAGC ACAGCCAGAG GCCCCAGGTT TGACTGTTTG GCAGTTTCCT 660
CGGGAACCGA TACAGCATGA GGCACACACC CATGGGGGAT GGCCAGGGGG TCCTTGAAGA 720
AGTCCTTTGC GGTGGAGGAC ACTCCAAGGA AAGTCCTTGA CCCAGGGGAA CCACCCACTG 780
AGGGTCCTTA AAGCACACAC TTCCCAGGAA ACCAACCCCT CACAGCAAGC CCGGGAGGTC 840
ACACCGCCAG CCCAGCAGAA CCCCTGGCAT CTCCTGCAGT GCTTCCGTGA CCGCCCCAAG 900
CTCAGACCTC AAAGTCCTCC CTCCAAAAGC AGCCTCAGAG CCTTCTGGAA GTCAAGGGCA 960
GACTGCCAGG ATACGAGCAC AGCAAGAAAG CAGGTGCCCT CCCCTGCAAA CCCTCCTCTG 1020
CACCCTCTCC GCTGCCTGCC TCTCCTTGCA CCCTCTCCCC TGCACCCTCT CCCTGCAAAC 1080
CCTCCCCTGC ACCCTCTTCC CGCACCCTCT CCCCTGCTCC CTCTCCCCTA CGCACCTTCC 1140
CCTGCACCCT CTCCTCTGCC TGCCTCCCCC TGCACGCTCT CCACTCCCCA CCTTCCCCTG 1200
CCCACCTTCC CCTGCACCCT CTCCCCTGAA CCCTCTCCTC TGCCTGCCTC CCCCTGCACC 1260
CTCTCCCCTC CCCACCTTCC CCTGCACCCT CTCTTCTGCC TGCCTCCTCC TGCACCTTCT 1320
CTCCTCCCTA CCTTTCCCTG TACTCTCGTC TGCCTACCTT CCCCTGCACC CTCTCCCCTC 1380
CCCACCTTTC CCTGCACCCT CTCCCCTGCA CACCTTCCCC TGCACTCTCT CCTCTGCCTA 1440
CCTTCCCCTG CACCCTCTCC CTCCCCACCT TTCCCTGCAC ACCTTCCCCT GCACCCTCTC 1500
CTCTGCCTAC CTTCCCCTGC ACCCTCTCCC CTCCCCACCT TTCCCTGCAC CCTCTCCCCT 1560
GCACACCTTC CCCTGCACCC TCTCCTCTGC CTACCTTCCC CTGCACCCTC TCCCCTCCCC 1620
ACCTTTCCCT GCACACCTTC CCCTGCACCC TCTCCCCTGC ACCCTCTCCT CTGCCTACCT 1680
TCCCCTGCAC CCTCTCCCCT CCCCACCTTT CCCTGCACCC TCTCCCCTGC ACACCTTTCC 1740
TTGTACCCCC TCCCCTCCCT AACTTCCCCT GCACCCTCTC CTCTGCCCCT CCTCCCCTGC 1800
ACACATCACA TACACACAGC CCTCTGGCCC ATGTGCACCT GCACAGAGCT TCAGTCTCAG 1860
CCCGTGTGCA CACTTGCACC TCCTACACAG CACACTTCCT ACCACACACA CCTCCCATTA 1920
CCACTGCACA CAGCTTAGGC TGCAGACCCC TCACACAACT GTTGAGTATA TACAACACCC 1980
ATTGCAACGC TTGTCACAGA GCCTAGGACC ACAGGCACCC CACAGCACAC ACACTGCACC 2040
TGACACCCAC CCTTGGCCGC TGATGCGACA CAGCCTCCTG CTGCCCCTCG CTCTGTCTCA 2100
CACACACATG CACACACATG CATATGGGTC TTGGGCGCCG TGGGCCTCCT CTCAGCCAGG 2160
CCCTGACACA GGCTCACTCA GAGCAGCGGG GAAGGCAGTC 2200
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