| Tag | Content |
|---|
EnhancerAtlas ID | HS007-09792 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr2:228315050-228316880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr2:228315171-228315189 | GTTTCCTTTCTTCTTTCC | - | 6.33 | | EWSR1-FLI1 | MA0149.1 | chr2:228315175-228315193 | CCTTTCTTCTTTCCTTCC | - | 7.74 | | HNF1A | MA0046.2 | chr2:228315297-228315312 | TGTTAATGTTTAATT | - | 6.48 | | MEF2A | MA0052.3 | chr2:228316769-228316781 | TCTATTTTTAGT | - | 6.27 | | MEF2B | MA0660.1 | chr2:228316769-228316781 | TCTATTTTTAGT | - | 6.32 | | MEF2C | MA0497.1 | chr2:228316768-228316783 | TTCTATTTTTAGTAG | - | 6.57 | | Nr2f6(var.2) | MA0728.1 | chr2:228316817-228316832 | TGAACTCCTGACCTC | - | 6.22 | | ZNF740 | MA0753.2 | chr2:228315158-228315171 | CCCCCCCCCCCCC | + | 6.03 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_28342 | chr2:228314003-228317657 | Fetal_Intestine | | SE_29240 | chr2:228314008-228317822 | Fetal_Intestine_Large | | SE_35773 | chr2:228314622-228317736 | HepG2 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I227449 | chr2 | 228314135 | 228317575 |
|
Enhancer Sequence | CTTATTTCCT GTTTGGGAAA AATACCGCAC TATGCTTCCT AGATTCAACT GAATTATGAA 60
ATGCAGAAAT TGAAATGGGT ACAAAAAGTA TACTATTTTT TTATCCCTCC CCCCCCCCCC 120
CGTTTCCTTT CTTCTTTCCT TCCTTTTTTT TCTGACAGCA TTCACACATA GAAGAAAAGT 180
TGATTCAATG CATCTGGATT GTGAAATAAA GCATAAGGTG TGGACAGGCA GTACAAGTAT 240
TGCATACTGT TAATGTTTAA TTAAATATTT GAAATCAAAC AGTTGACTTA GCAAGTGCTA 300
TAAAGAAGAG AGTGTAGATT TTACTAGCTT CTCCATAGCT TGGAAAAAAA TTCAGATTGT 360
ACCAACCAAG GACAGGTTTT CAGTCGTAAA AGCTAAACAT TATTCCATGG ATGGCTCCTA 420
GTGGGTGACT TTGGCTCCCT GGCTGCACTG CCCATGTGAC TTTACAGATC AGAAAACATC 480
TTCTACTAGG CGAGTTAAGA GGGGGTCAGA CCAATGAGTG GCTAATTTGT AAGGATTTCA 540
CTTAACTGAA AGACACCCTT CTGAGTGCTT TCTAAACCCC ATTAACAGAA ATTAGTGTTA 600
AAAGTTAAAA ACCAGTAATA ATCTGACCTT CAAGCATGCT ATACTATAAA CTGAACTCTC 660
TATTTTCTGG CTACTGCATT TTCCACTACC AGCCCTAGCC CAGGTTGCTT CCTCTGCCTG 720
AGATGTTCTT TCCTCCCAGC GCCATGTGCA CTCCAAATCC TGCCCATCTT AACTGCTACT 780
TCCTCCAAGA AGTCTCCCTT CCCTTATCCT TCAAGACTGA GGGACTCATG CCTTCCTGTG 840
AACTGCCTTA GTGAATTATC TCACCCCTCT TGTGACACTT CACTTTCTGT CTTGTTTTAA 900
GATCTTTTGT GTTTCCTTTT TTATTCCATT TTATTATATA AAAGTCCTTT GTGGAAAGGA 960
CTTGCACCTG GTTCCTTGTT CCATTCCCCA CACCACATGG CTCGGGACTT TGTACACTGT 1020
TTAGCAGATA ACAATTTAAA TGAATGACCC ATTAGATATC ATGTTGGTGT CTGATATTTG 1080
TTCTACCCAG AGTGAGTCCA TCTGGAGGGT GAGATAATGT CGTTCAGCTC CTTTCCAACC 1140
CCATCAGCAG TCCTAGGTGA AGAAAGGCAA AGGCCTGTTA TAGATCAACT CCCTGGACTA 1200
ATGTTGCAAT CATTCTCTTT GCAAACATGT GTCAGCGTTT CTGCTTCCAT ATCTTTCTAC 1260
ATATCCGCAG TGAACAAACT CCCTAAGAAA CACTGGCTTA TTGAAATGGG GCATGTTACT 1320
AAATACACAG CATTCTTTTT ATCTCCCTTC TCTGCTGTAT AACACACCAA CCTCCACTTG 1380
CACATTCAGA AATATAAAAA TGATTACATT ATGTAAATCC AACCCCTTTG TAGGGATCAC 1440
TGCCAGAGAG ATGTTAAAAT GACATTACAC CTGACCTTTC TGAAAAGGAT AATGCTCCAG 1500
AAGTAAATTC TTACAAATGA GGATGGACAA CACTTGGAGT TCTTTTTTTT TTTCTTTTTT 1560
TTTTTTCTTT GGAGTCTCAC TCTGTCACCC AGGCTTGAGT GCAATGGTGT AATCTTGGCT 1620
CACTGCAACC TCTGCCTCCT GGGTTCAAGT GATTGTCCTG CCTCAGCCTC CTGAGTAGCT 1680
GGGATTACAG GCGCCTGCCA CCATGCCCAG ATAATTTTTT CTATTTTTAG TAGAAATGAG 1740
GTTTCACCAT GTTGGCCAGG CTGGTCTTGA ACTCCTGACC TCAGGTGACC CACCTGCCTT 1800
GGCCACCCAA AGTGCTGGGA TTACAGGCAT 1830
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