| Tag | Content |
|---|
EnhancerAtlas ID | HS176-19791 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:20777260-20779990 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr2:20779461-20779475 | AGTCCCACGGGAAT | - | 6.01 | | NFE2L1 | MA0089.2 | chr2:20779231-20779246 | GCATGACTCATCAGT | + | 6.26 | | TFAP2C | MA0524.2 | chr2:20777681-20777693 | TGCCTCAGGGCA | + | 6.18 |
|
| | Number of super-enhancer constituents: 33 | ID | Coordinate | Tissue/cell |
| SE_00252 | chr2:20777587-20781075 | Adipose_Nuclei | | SE_00875 | chr2:20777193-20780159 | Adrenal_Gland | | SE_01560 | chr2:20777104-20780268 | Aorta | | SE_03248 | chr2:20778851-20780021 | Brain_Angular_Gyrus | | SE_03957 | chr2:20777502-20780166 | Brain_Anterior_Caudate | | SE_05080 | chr2:20777321-20780424 | Brain_Cingulate_Gyrus | | SE_05880 | chr2:20776875-20781185 | Brain_Hippocampus_Middle | | SE_07306 | chr2:20778329-20780235 | Brain_Hippocampus_Middle_150 | | SE_07924 | chr2:20777875-20781156 | Brain_Inferior_Temporal_Lobe | | SE_26682 | chr2:20777960-20780158 | Esophagus | | SE_27973 | chr2:20775677-20777611 | Fetal_Intestine | | SE_27973 | chr2:20778080-20780172 | Fetal_Intestine | | SE_29010 | chr2:20775624-20777732 | Fetal_Intestine_Large | | SE_29010 | chr2:20778147-20780228 | Fetal_Intestine_Large | | SE_30023 | chr2:20777612-20780174 | Fetal_Muscle | | SE_31621 | chr2:20775912-20777626 | Gastric | | SE_31621 | chr2:20777799-20780192 | Gastric | | SE_33420 | chr2:20778091-20780181 | H2171 | | SE_35251 | chr2:20776665-20781321 | HeLa | | SE_37942 | chr2:20765354-20785913 | HUVEC | | SE_40480 | chr2:20777911-20780167 | K562 | | SE_40670 | chr2:20766731-20780277 | Left_Ventricle | | SE_42169 | chr2:20775741-20780279 | Lung | | SE_46601 | chr2:20777664-20780171 | Osteoblasts | | SE_46720 | chr2:20778380-20778703 | Ovary | | SE_46720 | chr2:20778705-20779635 | Ovary | | SE_47850 | chr2:20778895-20779597 | Pancreas | | SE_48588 | chr2:20776905-20780113 | Right_Atrium | | SE_50417 | chr2:20775896-20780176 | Sigmoid_Colon | | SE_52547 | chr2:20777559-20780186 | Small_Intestine | | SE_53551 | chr2:20777658-20780109 | Spleen | | SE_54496 | chr2:20778077-20780207 | Stomach_Smooth_Muscle | | SE_65409 | chr2:20777658-20779864 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I020566 | chr2 | 20766626 | 20781108 |
|
Enhancer Sequence | TCCCTGCATT TCCTGTGACA TGTTAGCGGC TTGGAGGTGT CCCCCCAGCT CCACCAGGGG 60
CATAGGAAGA AAGAGCCTCC AGGCCCAAGG TGAGGGGCAC CTCCCAGCAC CGCCATCTGG 120
GAGCGTAAGA GTGCCTGTCT GTGGCTGCAG CCTGGGAGGG AGAGAGGGTC CAGAGATGGA 180
GGCAAGCAGA GGCCAGACCA ACTCAGGCCG GGTGCATGAG CTGGAATTGC CAGGCCTCTG 240
AACCTCAGGC TAGGTCGCAT TCTTGGAGCA GCAGATTAAA GTATGAGGGG GTATTGTCTA 300
AGCTACACTC CCCGGCACTG GGGCTGGATG GGGATTGGGC TTCCAGGGTT CTGTTATACT 360
GATCAGATCA ATGATTCATA TGCTGATGTA TCAGAACCAC CTGCAAACAC ATTTCCAGGC 420
CTGCCTCAGG GCACTCGTTC CTCAAGCCTG TCCAGTGTGA CTTCAACCCC CTTCACAGCT 480
GAGTAGGTTG TGGCCAGGGG CCATGGATCT GCAAAGACTG AGTAACGTGC CTGATGTCTC 540
ATCATGATCC AGCCGGCTGG GGACCTCTGG CATGGAACAC TCCAAGCTGC ATCATGTCCC 600
CTCAGGCAAC TTGCTGATCC CTGGCAAGGG GTGCAGGAAG CAGGCTCACG TGGCTGTGCC 660
CTTGAATCAG GGCTCGGGAG AGTGGCACAG GGTGGGGGTG GGAACAGCCT CTCTTGACCA 720
GTGCCTAGCG TCCTACCTGT GGCTCCTAAG TGGCTCCAGG GCTGCCCTCA GAGGCGGGAT 780
GGGATGCAGT CTTCATAGGA GGGGACTTGG TCTCCATGGT TTTCAGGGCA GAGCCCCACA 840
CCTATTACCT GGGCCCTGAG GCTCTACCCT AGCATGTCTC TCTGGGCTGT CCTCTGAAAA 900
GTTGCTCACC ATGGTAACCA ACCAGAAGTA GAGCCCCAGC TGAGGGCAGT GATGACACCA 960
TCTTTGGCCC TTGGACAACC GGGGCAGTTC TTGCCCGGAG GCTCTCGCAG GCAGCCCCAC 1020
ACACCACCTA TATCCCGAGG AAAGATGGGC ATTCCCAAGG AACATGTTCA GGCCAGACCC 1080
TCTGGGAGGT GAATAAGAAT AGATGCCCAG CCAAGAACCT CTTCAAAGCT CAAGAGGAAT 1140
GAAGAGAAGA GAGAGGACCA CCATTCACTG AGGGCTGGCC ATGGGTGAGG CACTGGGCGT 1200
AGGCAATCTC CTACATGCTC ATGACAGCCC TGGGAGCAGT ACTGCCACCT GCACTGGACA 1260
GGGGAGGAAA CTGAGGCTCA GAATGGGAAA GTAATTTGCT CAAGGCCAGA GTCCCTGGGT 1320
GTGTAGCTGT GACTCTGGAG CCATGCTCTG TATCAACCAG TGGGGTGTAC ATGAAACATC 1380
AACAGTAACA GCAATGTCCA GGTTCAAAAC ATTAAAAATA GCCTCAGTAC TACAAGGCTT 1440
TCTGTTTCTG AAACCTCTGT TGAAGGCAGC CAAGTGGAAA GTCAGGCGGT GTCCCCTCCC 1500
AAGCCTCACA GGCTGAGCCA GGTTTGGTGG CCACTGAAGC CCTTGACTTC CTTCCGGTCT 1560
CAGGTCAGTC CTCCCTGGGG CACTCCTAAT ATGCTCATCT GGAGGCTTCT GTTAAGTCCA 1620
GGAAACTCTA CAGGACACAG CTGAGGCTGG GCGGCCACCA GACACGTGCT GTGTCCAGAG 1680
AGAACAAAGC GGGGGTTTCC CTGGGTTCCA TGAGCACAGG AGCCTTTTCC TCCAGGCTGG 1740
CTCCATCCGA GCTGGCTGAG GGTTGGCGGC AGCTGCCCAG CATCTATAGG GTGCCTCCGG 1800
GAACTGTCTC AAGGCCAGAG CATCCAGCCT CCTGGCTGTT AGTGGGCCGT GAGCCTACCG 1860
GGACTTCGAG AGACAGGGCT TCCCCAGATC CAGCCTGATG AGATCATCTG CCATTTCAGG 1920
CTGGGCTGAA AGATCCTCCG GCACAACAAA GCTGGGCCCA GGAGATATCC TGCATGACTC 1980
ATCAGTTGGC CATGCATTGG AGACTTCCGG CCCTCAGAGA AACCAGACAC AGAGAGCCAT 2040
TGTTTGCCTT GGAAGCCCCC CGGCATACCA GGCTCAATGG GGTCATTTGT GTTTTCTCCC 2100
TAGTCCTCCA TAACCCATAC TCTTTCTGGG AGGTGGGGGC CCACTGAGCT GCCTGGGACC 2160
CTGTGACAAG AGGAAAACCA ATACCAAGTC ACCTACCCAC AAGTCCCACG GGAATACCCT 2220
CCCTCCAGGA CCAGGGCCTG GCTGGGAAGC AGAAAACCTG GGTTCTGAGC CATGGTTTAA 2280
GTCTCCAAGA CTCACTGATT CTTCTGTCTT CATTTTTCAA ATGGAGAAAA TCATTCAAAA 2340
AAGACAAAGC TATTGTGAGG ATGACCTAAC GTAAGGCACA TAAAGTTCCA GGCTCAGGCC 2400
TTGCACCTAC AAAGGTTCTG CATGTGATCT TTCCTTCCCA CTTCTCTCTT CCTCCTGCCT 2460
TTAAAATGTA AGTGAAAATG TTTTGTTTGT GGATCTGTTT CTATCCTAAT CTACATACCC 2520
TTATCTAGGG CAGAAACTCC CTGAACTCAT ACCCACAGTC TACCCACAAT TTGGCCCACA 2580
CCCAGGGACA CAGCCCCAAG GGGGCAAGGA CTGGAGCAGA GGGCACACAG CCTAGTGGCT 2640
AAGCTGGGCA GAGATGCAAG AATAAGCAAG GCAAGGCTGA GGGCCTGCCC CTGGGTTTCA 2700
AACAAGCTGG AGGCCTTTAG AAACTTCCAA 2730
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