| Tag | Content |
|---|
EnhancerAtlas ID | HS187-07944 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr14:100658640-100660570 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr14:100660295-100660315 | GGGGTGGGGGTGGGGGTGGG | - | 6.27 | | 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 | TCAGGCCTCG GCAGGGTCCT CTCCCTTTGC ATCTCCTACT AGTCAGCTGT CGGTGGTGAT 60
GGCCCGTGCC AAGTTCACGG TCTCAGCCTG ACGAAAGGCG GCCTTTACCA GCCTCAGGAC 120
CCCCAACGAA CCTGGGGCCA TGGCTGGGGA GGGGGCTCTG CCCAGGCTCT GCGTTCTGGG 180
ACAGGGGTCC CCAGATGGCC ATGCGTCAAG GCCCAGGGAC CTGTTTGTGG GCCCGAGAGC 240
ACGGGGGTCA GGGGTGGGGC TCGAGTCTCG TCCCAGGGCT CCGGGACAAG CTTCCTGGAG 300
GAGGCAGCGT GAGCTCTGGG AGGTAGAGGT CAAGACCTCA AAAAATGGGG GGACATGGGC 360
GGAGGGGGCA TTTTGTAACT CCTACGTCCC TGCAGAAGCC CAGACCCTCA GAGACTAGGA 420
ACTGAGGCCT GGCAGAGTGG GGTGGGCCAG CAATCACGCG CCAGGCCACA CGAGGAGAGC 480
CCACTGCCCC GGGGATGTCA GACGCGGGGC GGCCTCGGCG ACCGCACACG CCATAGAAAG 540
GTCACCGAAC TTGGCCGCCC GGCCGTCCCG GAAATCGCTA CTGCCCGGCA GCCCTGGGGC 600
CTCCACAACC GCGTCCCGGC GGCTCAAGTT GCCCTTTGTC GCCCCCTGCC GACCAGTCTC 660
CCTGCGGCTC CCGCGCGGGA CAATCAGGCG GGCCGGGCTC GGAAATAGTG GGCATGGGTC 720
CCTGAGGCGC GGGGATTGGC CGCTCTGTGT CATGTGTCCT CGGCTCGGGC CAACCAGCGA 780
GGGAGGCAAA GTCCCATCCC GCGCGTCCCG TAGCCCTTCA GCGAGCTGTG GGCGGGGCGT 840
CAGGCCTGAC ACCTCGGCCA GAGGGCGGGG CCGGAGACCT GAGCGGCGCC GCTTCCGCTC 900
TTTCGCCCAG GTGCCTTGGA GCCGCTGCTC TCGCCTCCCT TCTCCACCTA GCGGCGGTGT 960
TTCACACCCC GGAGTGGCTT TTTGGGGATA AAGGCACAAA TCTTTGCCAG ACCTCCCGCC 1020
AGGCCCCCTG GCCTGCCACG TGCTCCTTGC CGGCCTAGAC TCACCCAGGC TGTGCCCTCT 1080
GCTCAGAACG ACCTTTCCCC CCTTCCTCTC CCCCTCGCTT GCTCCGACTG TTCTTTGCAA 1140
TCCCGGCTGG GGTTGGGTTA AGGGCCTTCT GGGGCTTCTT CATACCCTGT GCATCTTCCT 1200
CCTACTGGCA CCGACCACCC CACACTGGGC TGCCATCTGC TTGTCTACAC CCACTGACTT 1260
TTCATCTCTG TATCTCCCCA GTAAGCAGGA GTGGCTCACA GAAGGCACGT TAATACCTGT 1320
GTGTTAATAT AAACCAAGGA GCGGGACGAT AGCTAGGAAG TAACATCCCT GGGCATCATC 1380
TGAGTACCAG GCCCCCTGCC AGGTACTTTA GAGGCTACTT GATGTTCAGG CCCATGGCAG 1440
CCCTGGGAGG GAGGCACAAA GGCTCTTTTG TTCCTGGGGA GTCAGTGGAG GCCCCTAGAG 1500
GCTGAATGAC TGTCTGGGTC CCCCAGCTGG ACTGTTTGGG GACAGGCCTG GGGAGCTGAG 1560
GGCACCCTCA TACCAGGCAG CCTTGCGCCT GAAGCTCTGC TGGTGAAAAC TGATGGGCAG 1620
GGCCCTGGAA GGGAGAGTCA GCGCCTGCGG GGGCGGGGGT GGGGGTGGGG GTGGGAAGGC 1680
AAGCGGAGGG GAAAGGTGAG CATAGACAGG CATTTGTGAT GGCCACAGGC CTTCACTGCT 1740
ACCCTGACAT CAGGGCCAAT GGCAACCTGC AAGGCCCTTC AAAGCCCTGC TTCCACCTCT 1800
GCCCATCTCT GGCTGCAACC TCCTGGTTCT CCCACCCTGT GCTCTATTCT CCAGCTACAC 1860
TGACCCATGT CAGCTCCCAG GCCATGCATC TGGGCCTTTC ACATGCTGCT CTCTCCAGGG 1920
TCCATCCAGC 1930
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