| Tag | Content |
|---|
EnhancerAtlas ID | HS091-38993 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr5:131769720-131772000 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr5:131771883-131771894 | CCACACCCTCC | + | 6.32 | | Klf1 | MA0493.1 | chr5:131771881-131771892 | GGCCACACCCT | + | 6.32 | | RREB1 | MA0073.1 | chr5:131770856-131770876 | GCCCATACCAACCCCAACCC | + | 6.1 |
|
| | Number of super-enhancer constituents: 37 | ID | Coordinate | Tissue/cell |
| SE_00037 | chr5:131769476-131776420 | Adipose_Nuclei | | SE_09163 | chr5:131769539-131776436 | CD14 | | SE_11905 | chr5:131771443-131772099 | CD3 | | SE_18258 | chr5:131771017-131776294 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19103 | chr5:131771175-131772281 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_19972 | chr5:131769618-131776268 | CD56 | | SE_22284 | chr5:131754357-131780344 | CD8_primiary | | SE_23079 | chr5:131769694-131771398 | Colon_Crypt_1 | | SE_23079 | chr5:131771568-131772123 | Colon_Crypt_1 | | SE_23750 | chr5:131770391-131770966 | Colon_Crypt_2 | | SE_23750 | chr5:131771062-131771423 | Colon_Crypt_2 | | SE_23750 | chr5:131771671-131772131 | Colon_Crypt_2 | | SE_25340 | chr5:131769678-131772094 | DND41 | | SE_25784 | chr5:131769540-131776186 | Duodenum_Smooth_Muscle | | SE_26597 | chr5:131769999-131771102 | Esophagus | | SE_27859 | chr5:131769639-131772128 | Fetal_Intestine | | SE_28909 | chr5:131768454-131771973 | Fetal_Intestine_Large | | SE_30917 | chr5:131769816-131771306 | Fetal_Thymus | | SE_31393 | chr5:131770034-131771484 | Gastric | | SE_39368 | chr5:131770545-131771502 | Jurkat | | SE_39368 | chr5:131771530-131772102 | Jurkat | | SE_40726 | chr5:131769888-131771252 | Left_Ventricle | | SE_40726 | chr5:131771413-131772138 | Left_Ventricle | | SE_42103 | chr5:131769872-131772151 | Lung | | SE_48659 | chr5:131770097-131771409 | Right_Atrium | | SE_50034 | chr5:131769767-131771423 | RPMI-8402 | | SE_50051 | chr5:131769920-131772121 | Sigmoid_Colon | | SE_52336 | chr5:131769663-131772128 | Small_Intestine | | SE_53285 | chr5:131769955-131770781 | Spleen | | SE_53285 | chr5:131771498-131772157 | Spleen | | SE_54554 | chr5:131769980-131771486 | Stomach_Smooth_Muscle | | SE_56265 | chr5:131771323-131776703 | u87 | | SE_59850 | chr5:131745223-131774088 | Ly4 | | SE_61542 | chr5:131744876-131774119 | Toledo | | SE_62219 | chr5:131721125-131837948 | Tonsil | | SE_66244 | chr5:131770545-131771502 | Jurkat | | SE_66244 | chr5:131771530-131772102 | Jurkat |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 131770427 | 131770908 | | chr5 | 131771667 | 131772000 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I132433 | chr5 | 131769658 | 131776999 |
|
Enhancer Sequence | GCCTCAGTCT CCCAAAGTGC TGGGATTACA GGCGTGAGCC ACCACTCCCG GCTAGCAACC 60
GGCTTTTTAC AAATAGCAGT CTATTGTGTA TATTTCTCTA TGACAGTACA TAGAGACCTG 120
CTGTCTTCTT TTTAAAGGCT GCTTGGTATG TATTCCACCA CGTAGATGTA CTGCTAGTTC 180
ATCTCCTCCC CTACAGATGA CCACAAAGTT TTTCAATGTC CTGATAATAT TTATAGGCCA 240
CTACATCCTC ATTTTTATAC TTTTATGCAT TTGTGCTAGT GTTTCTATAA AATAGATTTC 300
TACAATTGAG ACTGTTGAGT TAAAGGGTAT ATACATAGTA AGTTGTATAT ACTTCCAGTT 360
GCCCCTTGTT GAAACCTTGT ACCAATCAGT GCAGTGTCCT TTTAAATGGT CTTTTCATTG 420
CCTGTTGCTT CCCTGTCTCC CCACCCCCCG GCTCTTCACC CTAGTGCTAG AATTGCTTTT 480
ATGAAACTCA GATCTGACCA TGGCTTGCCC TGTTTAAAAT ACCTCAGTGG CTCCTCACTG 540
TCAGCAAAAC CCAAACATTC ATCTAAGCTC CTTCTCAGTT GGAGTCCTCT GGGAAGCAGA 600
CACCAAAACA GAATGAAAAG TGCAGAAGAT TTATTGGGGG TAAGAAGAGC TAATGCCTAT 660
GAAAGATAAA GGAGAAAGGA GCAGAAGTAC GGAGAGAAAA GACAGCTTTC AGACTGCAGT 720
CCAGATCTAA CTCTGGGACG CAAGAGAGGG AAGGATAATT CTGTTGAAAG AGCATCAGAC 780
TGTGATGCGG CTGTAAGAGT GTCTCAACGA GCCCAGTGGG GAGTTCCAGC CAAAGATTGC 840
CCAGGAGAAG AGTCGCACTT TGGGCAGAAA TGGACAGGCC CGAGCAACCC TGCCATGTTC 900
TGTCATTGGC TGGGGGCCAC CCAGGAGGCA ACATGGTCTG ACTTGAATGG TGTGGATCCG 960
AGGCTGCAGC CTGTCAGCTG TCTGCACTCC ATGCAACAGG TCCTTTGAAT GGCATGTGTT 1020
CGTGGCTGCC ATAAACTGCA GCCTGCCTTT TAGCCTTACC TCCTTTGCTC TTGCTCTCTG 1080
ACCCCGTGTT CTGGCAACAC TGGCCTGACT ACACGCCGTA TCACATACAA CCAACTGCCC 1140
ATACCAACCC CAACCCTGAC CTTTGCTCAC TCAGTTCTTT CTGCCTGGAA TGCCACTCCT 1200
TCCCAGTTAT ACCCAGCAAA ATCCTAATGT GCTTTCAAGG CCCAACTTAA AAATCATCTT 1260
CTCTGGTTGA CCTCACCATG TAGAATTAAT TGTTCCTTGC TCCTATGGTG CTATGTGTAT 1320
ATTAGTACTT CCCAGATTGG AGTATTCTTA GCTGTTTTTT TCTCAGATTT TTGCCTCCTC 1380
TAAACCTAGC AAAACGTCAG CACACAGTAA ATGTTGACTG AGCTGTTTCC CTGCTCCTCG 1440
CAAAGCACCT TGAGGTTGCA GAATTCCAAC TCCCGGAATG GTTGGAAGCA CACAGTACAT 1500
GGTCAATAAG TGTTTGTTGA CTTGTCTGGG ACCTAGTATT GGTGGGGTGA GGTGGGCAGA 1560
AGGCTGCTGA GGGTGGGTAT TTACTGTTGT TGGGGCTCAC CAGTCTGGGG CCACATTGGA 1620
GTTTTAAGAC TAGAGCATGT CTTCCCCTGT TTTTATTTTT CTCCATGATT TGGAAAGACC 1680
CCAGAGGTGG GTTTTTTTTT TTTTAAGTAA TCACTTTATT GTCTCTGGTC AACAAATGAG 1740
AACTTTTATG GGTCTTCCCT TTTTCAACCA CATTTTCATG AGTTGGGATT TTGCATTTCT 1800
TCATTACCCA TTCTCCTTAT GGGTAAAAGA AGAGCCATTA TGATACCTAG GATGAGAGCT 1860
CCAGGTCAGA TGGGTAATCA TTTTCAGACT GGAGGCTCAT GGGATACAGG GAATTGGGAA 1920
GGTAGAAATG ATATTTTTCC TCTTCCTCTT TCCCACATCC ACCAATTAAA GAACTTCCCT 1980
GGGAGTGGAC CTGTGGGAAG TGGCTAAGGG TTTCCGGGGT GGGTACAGCA GGGAGTGACA 2040
TCAGGGCGTG GTGGGGATGA GGTGGGTGGA GAGGACAAAG AGGGACTCTC CACCTTCCTT 2100
TGGATCTATG AGGATGTTCC TTGGCCACTG TCCCTCAGCA GAAGGAGGCT AGAGCTGAGG 2160
TGGCCACACC CTCCACTCAT TTTCAATCCC TTCAAACTGT CAGGCCCTCA GAGGAAACCC 2220
TAGGGTTTCC CCACCAAGAT GTAAGGGCTG TGTGCCTCTG CCTTCTCTCT TAGGGTGGTC 2280
|
