| Tag | Content |
|---|
EnhancerAtlas ID | HS030-05496 |
Organism | Homo sapiens |
Tissue/cell | CyT49 |
Coordinate | chr12:89772370-89774820 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:89774247-89774265 | CCCTGCTTCCTTCTCTCC | - | 6.14 | | EWSR1-FLI1 | MA0149.1 | chr12:89774239-89774257 | CCCTCCTCCCCTGCTTCC | - | 6.22 | | FOXA1 | MA0148.4 | chr12:89773317-89773333 | ATTTGTTTGCTTAAGC | - | 6.37 | | STAT3 | MA0144.2 | chr12:89773847-89773858 | TTTCCCAGAAG | - | 6.62 | | ZNF263 | MA0528.1 | chr12:89774196-89774217 | CCCTTCTCCTCCTCCTCCTCC | - | 10.3 | | ZNF263 | MA0528.1 | chr12:89774193-89774214 | TCCCCCTTCTCCTCCTCCTCC | - | 10.66 | | ZNF263 | MA0528.1 | chr12:89774199-89774220 | TTCTCCTCCTCCTCCTCCTCC | - | 10.92 | | ZNF263 | MA0528.1 | chr12:89774208-89774229 | TCCTCCTCCTCCCTCTTCCCT | - | 6.09 | | ZNF263 | MA0528.1 | chr12:89774227-89774248 | CTCCTTCCCATTCCCTCCTCC | - | 6.21 | | ZNF263 | MA0528.1 | chr12:89774209-89774230 | CCTCCTCCTCCCTCTTCCCTC | - | 6.28 | | ZNF263 | MA0528.1 | chr12:89774181-89774202 | TCCCCTTCCCCCTCCCCCTTC | - | 6.29 | | ZNF263 | MA0528.1 | chr12:89774206-89774227 | CCTCCTCCTCCTCCCTCTTCC | - | 6.32 | | ZNF263 | MA0528.1 | chr12:89774172-89774193 | CTCTTCCTCTCCCCTTCCCCC | - | 6.3 | | ZNF263 | MA0528.1 | chr12:89774213-89774234 | CTCCTCCCTCTTCCCTCCTTC | - | 6.69 | | ZNF263 | MA0528.1 | chr12:89774230-89774251 | CTTCCCATTCCCTCCTCCCCT | - | 6 | | ZNF263 | MA0528.1 | chr12:89774242-89774263 | TCCTCCCCTGCTTCCTTCTCT | - | 6 | | ZNF263 | MA0528.1 | chr12:89774239-89774260 | CCCTCCTCCCCTGCTTCCTTC | - | 7.35 | | ZNF263 | MA0528.1 | chr12:89774184-89774205 | CCTTCCCCCTCCCCCTTCTCC | - | 8.16 | | ZNF263 | MA0528.1 | chr12:89774178-89774199 | CTCTCCCCTTCCCCCTCCCCC | - | 8.18 | | ZNF263 | MA0528.1 | chr12:89774187-89774208 | TCCCCCTCCCCCTTCTCCTCC | - | 9.51 | | ZNF263 | MA0528.1 | chr12:89774202-89774223 | TCCTCCTCCTCCTCCTCCCTC | - | 9.59 | | ZNF263 | MA0528.1 | chr12:89774190-89774211 | CCCTCCCCCTTCTCCTCCTCC | - | 9.98 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_25078 | chr12:89772554-89773143 | Colon_Crypt_3 | | SE_25078 | chr12:89773857-89774397 | Colon_Crypt_3 | | SE_27644 | chr12:89771389-89775687 | Fetal_Intestine | | SE_28566 | chr12:89761572-89775819 | Fetal_Intestine_Large | | SE_35767 | chr12:89772428-89774396 | HepG2 | | SE_50215 | chr12:89772425-89774424 | Sigmoid_Colon |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I089368 | chr12 | 89761900 | 89775589 |
|
Enhancer Sequence | TGGCTAACAC GGTGAAACCC CGTCTCTACT AAAAATACAA AAAATTAGCT GGGCGTGGTG 60
TCGGGCGCCT GTAGTCCCAG CTACTTGGGA AGCTGAGGCA GGAGAATGGC GTGAACCTGG 120
GAGGCGGAGC TTGTGGTGAG CTGAGATCAC GCCACTGCAC TACAGCCTTG GTGACCGAGC 180
AGGACTCCAT CTCAACAACA ACAACAAAAA TACAAACAGA AAATTCAAGT ACTGCAGTGG 240
AAATATGATG GAGTTTCTAT CAAATTATAT CAAAAGTTGT TCTGGGGAGA ACTTAAACCA 300
ATTCAACAGC TCAAAAGGAG GGCATGAAAC CCACTCCTCC CACCTCCAGT AGCACTCCTT 360
TTACTCATTT TTTTCCCCTT CTCCAAAATT CTAAACTGCT CACGCATTCC AGATTGTTCC 420
TGAGGAGAAT GAGCATATGC TATCCTGGTG TGGAAATGCC TGGTATGCTA ATTCATAGTT 480
TGGAGGAGAG AGAAGATATG AGGTCGAACT GGAAGATAGT GAACTAAAAA TAATATAACC 540
CACCTCCATG CCTCTCTCTT TAGCTCAGTG CCACATCTTC CCCTGCCAAA GGGAAGCCAC 600
GGCGCCACAA CATCCTGAGG AGAGAGAGCC TTGATTTTTC TGTTGGGGAC CCACTTTTCC 660
CCTATAGGAG AAACGACCAT CAATCACAAT ACCTTCCCCT ATCCTGGCCA AAGGGAGGTT 720
GGATCCCTAG CTGAAGGTAG GCCTATCAGA TACTCTTGAC CTGGAATTTC AGTGTGGAGA 780
GAAGTGACAC AAAAACTGAG AATGGTTGGA AATCATTTAC CCTGGAGGCA ATGAAACTAA 840
GGAAACTGCA TTATTCACAA AACCTGAATT TCTAGAGCTT CTCTTGTCCT TGAATAAAGC 900
AGATTCTTCA GCCTCTCCTT CTGTGAGATA CTCTATCCTT CCGATAAATT TGTTTGCTTA 960
AGCTATCCAG AGTCAACTTC TGTTAACCTC ATCACAGAAT TCTGATGAAA ATAGCTTCTC 1020
AGATGCTTCA GGCTCCAATA TGCAATGCTA AAGGTCAAAA TTTAGGGGTG GGGGAGGAGT 1080
CACTTGGGTC AAACATTTAC TAAGGCACCA AGCTCAATTT TTCTGAAGAC ATTCTTCTCC 1140
CAGAGGTTGG CTTTATGGCA TCCCTTACAG AGCGAGGGCC GCACAGGCCT GGGAAGGAAA 1200
AGGAGCCCCT GAGTCCATCT TTTCCTGCAA CTAATTTGGT TAAAATCACC AGATTCCCTA 1260
ATTCTCCTAA TGCAATTCCA ATGAGTCCCA CAGATTCTAG AAAAGTGTCA GTGGTGCTGG 1320
TCTAGGTGGG TAAGTTTCAA TCTGTCTTGT AAGAGGCAGT GACAAAGTTA CACAGTAATT 1380
ATATAACAGA TTATGGTGGA GAAGCAGCCG CTGCCTTTAA AAAAAAAATC ACTGCGTGGG 1440
AACTTTTCAA ATCACAACCC TCCATTAGAA GCCTATATTT CCCAGAAGAT CCTCATTCCT 1500
TCATTTAGGC AGCAGTTTTA AAGTCAGCTG GAACCACTGT TTCCTCATGA CAGCAACGGA 1560
AAGGGCCAAA CTGTATCTTA TTTTACTAAA TAAGCAGCGT GTCCTAGTCA TGGCACTTTG 1620
TATCCCTAGG ATGTCACCTT GTTTTGAAGT TATTTCAGCT TTGGTTTGAA AAGTATCCTG 1680
TCAGCAAAAC CAGCCTTCTC CCCATGGAGT TTAGGAGCCA GGAGGGAGTA AGGGAAGGGA 1740
TGCGTAGGAG ATGATGTTCC TGAATCATTT ACCAGGAGCC CTCCACCTGT TGAAATTATG 1800
TTCTCTTCCT CTCCCCTTCC CCCTCCCCCT TCTCCTCCTC CTCCTCCTCC CTCTTCCCTC 1860
CTTCCCATTC CCTCCTCCCC TGCTTCCTTC TCTCCCTTCT ACTTCTCGTC TTTTATTTAT 1920
TTGGTTTTGC TGCAGGTGCA ACTCCAGTAT CCTGATGGGG GAAGCAACTT AAGTGTTTTT 1980
TTGTTTTTTT AAAACAGAAT CTCACTCTTG TCCACCAGGC TGGGGTGCAG TGGCATGATC 2040
TGGGCTCACT GCAACCTCTG CCTCCTGGGT TCAAGCGATT CTCCTGCCTC AGCCTCCTGA 2100
GTAGCTGGGA TTACAGGCAC CCACCACCAT GCCCAGCTAA TTTTTGTATC TTTAGTAGAG 2160
ACGGGATTTC ACCATGTTGG CCAGGCTGGT CTCGAACTCC TGACCTCAGG TGATCCATCC 2220
GCCTCGGCCT CCCAAAGTGC TGGGATTACA GGTGTGAGTC ACTGTGCCTG GCCCAGTGTA 2280
TTCTTTTATT CAACAACATT TGTTGAGTAT CCTGGACCAG GTACTGGTAA ACTAGATAGG 2340
CAACGTCCTT GCCTTGGAGG AGCTTCTATT CCAATGGAGG GAGACAGAAG CCAATGATGA 2400
TTTCAGATCT GCTTGGCCCA CAGGGAGCCC CTGGGTCTAA CATATGGGCA 2450
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