| Tag | Content |
|---|
EnhancerAtlas ID | HS108-12598 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr14:100658420-100660800 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr14:100660295-100660315 | GGGGTGGGGGTGGGGGTGGG | - | 6.27 | | RREB1 | MA0073.1 | chr14:100658428-100658448 | CCACCACCCACCCACTTCCG | + | 6.57 | | RREB1 | MA0073.1 | chr14:100658424-100658444 | CCCCCCACCACCCACCCACT | + | 7.63 | | ZNF263 | MA0528.1 | chr14:100659731-100659752 | CCTTTCCCCCCTTCCTCTCCC | - | 6.21 | | ZNF263 | MA0528.1 | chr14:100659733-100659754 | TTTCCCCCCTTCCTCTCCCCC | - | 6.41 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_23822 | chr14:100658575-100659390 | Colon_Crypt_2 | | SE_23822 | chr14:100659435-100660335 | Colon_Crypt_2 | | SE_24776 | chr14:100658405-100660543 | Colon_Crypt_3 | | SE_27982 | chr14:100658545-100660323 | Fetal_Intestine | | SE_29025 | chr14:100658411-100660318 | Fetal_Intestine_Large | | SE_31574 | chr14:100658310-100661006 | Gastric | | SE_35748 | chr14:100658539-100659393 | HepG2 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I100192 | chr14 | 100658488 | 100660354 |
|
Enhancer Sequence | CCCTCCCCCC ACCACCCACC CACTTCCGAA GTGGTCTAGG GCTTAAGTCC AGATGCGGAT 60
GGGCTCAGGG CGGGGTGGGA GAAGTCAGGG GAAAAAAAAA AAGAAAAGAA AAAAAAGATA 120
AAGAAATAAA TTTCTTCTGC CAGATACCTT AATTAATCAA GGTCGGCCTT CCATCAAGGT 180
CGGCTTCTCG GCTCCCCAGC CCCCGCGCCT CACGGGGACC TCAGGCCTCG GCAGGGTCCT 240
CTCCCTTTGC ATCTCCTACT AGTCAGCTGT CGGTGGTGAT GGCCCGTGCC AAGTTCACGG 300
TCTCAGCCTG ACGAAAGGCG GCCTTTACCA GCCTCAGGAC CCCCAACGAA CCTGGGGCCA 360
TGGCTGGGGA GGGGGCTCTG CCCAGGCTCT GCGTTCTGGG ACAGGGGTCC CCAGATGGCC 420
ATGCGTCAAG GCCCAGGGAC CTGTTTGTGG GCCCGAGAGC ACGGGGGTCA GGGGTGGGGC 480
TCGAGTCTCG TCCCAGGGCT CCGGGACAAG CTTCCTGGAG GAGGCAGCGT GAGCTCTGGG 540
AGGTAGAGGT CAAGACCTCA AAAAATGGGG GGACATGGGC GGAGGGGGCA TTTTGTAACT 600
CCTACGTCCC TGCAGAAGCC CAGACCCTCA GAGACTAGGA ACTGAGGCCT GGCAGAGTGG 660
GGTGGGCCAG CAATCACGCG CCAGGCCACA CGAGGAGAGC CCACTGCCCC GGGGATGTCA 720
GACGCGGGGC GGCCTCGGCG ACCGCACACG CCATAGAAAG GTCACCGAAC TTGGCCGCCC 780
GGCCGTCCCG GAAATCGCTA CTGCCCGGCA GCCCTGGGGC CTCCACAACC GCGTCCCGGC 840
GGCTCAAGTT GCCCTTTGTC GCCCCCTGCC GACCAGTCTC CCTGCGGCTC CCGCGCGGGA 900
CAATCAGGCG GGCCGGGCTC GGAAATAGTG GGCATGGGTC CCTGAGGCGC GGGGATTGGC 960
CGCTCTGTGT CATGTGTCCT CGGCTCGGGC CAACCAGCGA GGGAGGCAAA GTCCCATCCC 1020
GCGCGTCCCG TAGCCCTTCA GCGAGCTGTG GGCGGGGCGT CAGGCCTGAC ACCTCGGCCA 1080
GAGGGCGGGG CCGGAGACCT GAGCGGCGCC GCTTCCGCTC TTTCGCCCAG GTGCCTTGGA 1140
GCCGCTGCTC TCGCCTCCCT TCTCCACCTA GCGGCGGTGT TTCACACCCC GGAGTGGCTT 1200
TTTGGGGATA AAGGCACAAA TCTTTGCCAG ACCTCCCGCC AGGCCCCCTG GCCTGCCACG 1260
TGCTCCTTGC CGGCCTAGAC TCACCCAGGC TGTGCCCTCT GCTCAGAACG ACCTTTCCCC 1320
CCTTCCTCTC CCCCTCGCTT GCTCCGACTG TTCTTTGCAA TCCCGGCTGG GGTTGGGTTA 1380
AGGGCCTTCT GGGGCTTCTT CATACCCTGT GCATCTTCCT CCTACTGGCA CCGACCACCC 1440
CACACTGGGC TGCCATCTGC TTGTCTACAC CCACTGACTT TTCATCTCTG TATCTCCCCA 1500
GTAAGCAGGA GTGGCTCACA GAAGGCACGT TAATACCTGT GTGTTAATAT AAACCAAGGA 1560
GCGGGACGAT AGCTAGGAAG TAACATCCCT GGGCATCATC TGAGTACCAG GCCCCCTGCC 1620
AGGTACTTTA GAGGCTACTT GATGTTCAGG CCCATGGCAG CCCTGGGAGG GAGGCACAAA 1680
GGCTCTTTTG TTCCTGGGGA GTCAGTGGAG GCCCCTAGAG GCTGAATGAC TGTCTGGGTC 1740
CCCCAGCTGG ACTGTTTGGG GACAGGCCTG GGGAGCTGAG GGCACCCTCA TACCAGGCAG 1800
CCTTGCGCCT GAAGCTCTGC TGGTGAAAAC TGATGGGCAG GGCCCTGGAA GGGAGAGTCA 1860
GCGCCTGCGG GGGCGGGGGT GGGGGTGGGG GTGGGAAGGC AAGCGGAGGG GAAAGGTGAG 1920
CATAGACAGG CATTTGTGAT GGCCACAGGC CTTCACTGCT ACCCTGACAT CAGGGCCAAT 1980
GGCAACCTGC AAGGCCCTTC AAAGCCCTGC TTCCACCTCT GCCCATCTCT GGCTGCAACC 2040
TCCTGGTTCT CCCACCCTGT GCTCTATTCT CCAGCTACAC TGACCCATGT CAGCTCCCAG 2100
GCCATGCATC TGGGCCTTTC ACATGCTGCT CTCTCCAGGG TCCATCCAGC CCCACCTCCA 2160
CCACATTGCC AAGACCAGGC CTTACTTTCC AGACTCCATG TACTTCTCAG CACTGGCCCC 2220
ACCATTTGTG CTGAGGATCA TCAGCTACTG AGACCTGAAT TCAACCCCAG GCCCTGGGTT 2280
TGAATTCTGA CACATTTGTG GCTGACCTTG GAGAACAGCT CATCCATGGG CTCGCAAAAC 2340
AATGCCGCTG ACTTAGACAA CACTCTACTG ATTTGCTGGC 2380
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