| Tag | Content |
|---|
EnhancerAtlas ID | HS092-23978 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr2:47193360-47196300 |
Target genes | | Number: 15 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6 | MA0463.2 | chr2:47193953-47193969 | AATTCCTAGAAAGTAG | - | 7.14 | | BCL6B | MA0731.1 | chr2:47193951-47193968 | TAAATTCCTAGAAAGTA | - | 7.23 | | JUN(var.2) | MA0489.1 | chr2:47193617-47193631 | ATGAGTCATTTTTC | - | 6.68 | | Myog | MA0500.1 | chr2:47195102-47195113 | CTGCAGCTGTC | - | 6.62 | | Nr2f6(var.2) | MA0728.1 | chr2:47194135-47194150 | GAGGTCAGGAGTTCA | + | 6.22 | | Tcf12 | MA0521.1 | chr2:47195102-47195113 | CTGCAGCTGTC | - | 6.14 |
|
| | Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
| SE_00056 | chr2:47193106-47196568 | Adipose_Nuclei | | SE_00864 | chr2:47194770-47195906 | Adrenal_Gland | | SE_01547 | chr2:47194919-47195899 | Aorta | | SE_03864 | chr2:47194593-47196000 | Brain_Anterior_Caudate | | SE_04790 | chr2:47194452-47196092 | Brain_Cingulate_Gyrus | | SE_05773 | chr2:47194415-47196333 | Brain_Hippocampus_Middle | | SE_06717 | chr2:47194864-47196105 | Brain_Hippocampus_Middle_150 | | SE_07731 | chr2:47194478-47195922 | Brain_Inferior_Temporal_Lobe | | SE_09141 | chr2:47188826-47202968 | CD14 | | SE_26122 | chr2:47194205-47196331 | Duodenum_Smooth_Muscle | | SE_26616 | chr2:47194256-47196364 | Esophagus | | SE_34911 | chr2:47193577-47196531 | HeLa | | SE_36729 | chr2:47193948-47196530 | HMEC | | SE_43054 | chr2:47194681-47196092 | Lung | | SE_47823 | chr2:47194916-47195888 | Pancreas | | SE_53025 | chr2:47194788-47196340 | Small_Intestine | | SE_53323 | chr2:47194762-47195996 | Spleen | | SE_54495 | chr2:47194376-47195982 | Stomach_Smooth_Muscle | | SE_65159 | chr2:47193986-47196476 | NHEK | | SE_65882 | chr2:47194784-47196030 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 5 | Chromosome | Start | End |
| chr2 | 47194314 | 47194923 | | chr2 | 47196160 | 47196200 | | chr2 | 47194379 | 47194775 | | chr2 | 47195176 | 47195614 | | chr2 | 47193730 | 47195806 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I046963 | chr2 | 47190740 | 47199767 |
|
Enhancer Sequence | TACAGGTGTG AGCCACTGTG CTTGGCCTGC ATACTTTCTA CTCTTTATAA TATTTCATCT 60
AATTTAATGA TCATGGCTAC ACTACGAGCT AGGCATTATT AGTAACTCTA TTTTGTATTT 120
GCGGAAACAG ACTTAGCACT CTGTGAACAT TTTGAGGTAT ATCTTTCCAG TCTTTTTTCC 180
CTATAGGATT ATATATGCTT TTAAAATGTA AGTTCATACA GTCATGTTTT ATAATCTGCT 240
TTTTAAAAAA GTATTTCATG AGTCATTTTT CAATACACCT CTATGTCACT GTAAGTAACT 300
TCATAGCATT TCATTGTAAC GTTCTATCCT AATTTTGTGA AGTCCCGTCA TTGGACCTGT 360
ATGCTAAATC TTTTTTTTTT TTGCCATTAT AAATAATACT GAAATGGATA TCCTTGAAGC 420
TAAATTTTGT ATACATCACT TTTTTTTTTT TTTTGGTGGA GATGGGGTCT ATGTTGCAAG 480
GGCTGGTCCT GAACTCCTGG GCTCAAGCAA TCCTCCCACC TTACCCTCCC AAAGTGCTGG 540
GATTACAGGT GTGAGTCACC ACCCCCAGCT TTTTTTTTTT TTTTTCGAAG ATAAATTCCT 600
AGAAAGTAGA ATTACTGAAT CATAGAGTAT ACATTTTTTG GAGACTTTGA TACAGAAGCC 660
AAATTGCCTG TGTTTTTTGT TTTTTTTTTT TCCGTTAAAA AATTGTGTTG GCCGGGCGCG 720
GTGGCTCATG CCTATAATCC CAGTACTTTG GGAGGCTGAG GCGGGTGGAT CACCTGAGGT 780
CAGGAGTTCA AGACCAGCCT GGCCAACATG GCGAAACCCC ATCTCTACTA AAAATATAAA 840
AATTAGCCAG GCGTGGTGGC GCGTGCCTGT AATTCCAGCT ACTCAGGAGG CTGAGACAGG 900
AGAATTGCTT GAACCCAGGA GGTGGAGGTT GCCGTGAGCT GAGATTGTGC CACTGCACTC 960
CAGCCTGGGT GACAGAGCAA GATTCCGTCT CAAAAAAAAA ATGTGTTAAA TATACATACC 1020
ATAGAATTGA CCATCTTAAC CACTTTTAAG CGTACAGTTC GGTACTAAGA CACTGTTGTG 1080
CAACCAATCT CCTGAACTCT TTTAACATTT GCATTATTGT GCAACCAGTC TCCAGAATTC 1140
TTTTACCTTG CGAAACCAAA ATTCTATGCC CGTGAAACAG CAACGCCCCA TTCCCTCCTC 1200
CCCTAACCCC TGGCAACCAC TCTTCTATTT TCTGTTTTTA TGAATTTGAT TACGCAAGTA 1260
CCTCATGTAA GAGGAATCAT ACAGTATTTG CCTTTTTGTG TCTGGCTCAT TTCACTTAGT 1320
AAAATGTCCT CAAGGCTTAT CCATATTGTA GCATGTGTCA GAATTTCCTT CCTTCTGAAG 1380
GCTGAATAAT ATTGTATTGT ATGTATGTAT ATGTGGCATT TTGTTTATGT GTTCATCTGT 1440
CAATGGACAC TTGGGTTGCT TCTACATTTT AACTATTGTG AATAATGCTG CTATAAATGC 1500
TAGTGTACTA ATACCTCTTT GAGACCCTGC TTTCTATTCT TTTGGGTATA TACCTGGAAG 1560
TGGAATTGCT GGATCATATG GTAATATCTA TTTTTAAATG TTCTAATTTT AACAGAGTGA 1620
TCTGTGAGGG TTCTTTCCTA CCTGGCCTTT CGGTTTCCCC CCGAGAGCTG AATGAATTGC 1680
ATTTTTTCGC TTCTTCCCGT GGCTGCAGGG TACCCAAGTC TGGGATTCAT CTTCCGTGGG 1740
TGCTGCAGCT GTCCTCGTGC CCTTTGACAG GCTGGGTAGG TGGGAGGGAA GGGGTTCTGT 1800
TGCTGAGGAT GTTTTCTGTT TTCTACCTCT GCATCCAGGG CCCAAGGCTC CAGGGTTCCA 1860
AGGGTGGGGC TTCTTGGAAG GGCGGCTGCC TTGGATGTGA TGAGTCATTC AGACTGAAGG 1920
AGTTGGGACC AGCCTGGTGT TGGGCCTGAG GCTGTGCCAG GATCAGCTTG GCTCCAAATC 1980
GAAAGTTCTG AGTTAATGAA AAAGCAAGTC CTCCTCTTGC AAGGGACCTT TCCTAGAGCT 2040
GGGTATTGGC ACAGAAAGGC CCTTGCCGGT GGGAATCACA AGGCAGTGCC TGCCCTGCAG 2100
GGCTGTGTTA CAACCCTCCG ATGCCTCAAG GACTGGGCGC AGGGCAGCCC ACCTTCATCC 2160
TGGATTGAGC ACTGTAGTCT GGCCGTTTGT GCAGAAGCGC TCACGGGGCA GAAGGTAAAG 2220
AAAAGAAACC CAAGCCTGCA GCACCTGGGT GGGCTTCCAG TCAGATGTTT GTGGACAGGA 2280
AAATAGACCT TATCAACCAG GGGACAAATA CAAGGTTCCC GGCCCCTTTT TATGGGCAGA 2340
ACTGGGTGAC TGGACTGTGA CCTTGCTTAG GAAAAGCCAC TGCCAGCTCC AGAAACTTTT 2400
TGGCCCTGTG TATATTGGAA ATTGCTTTAT AGAGGACCGC CTCCGTGAAT GTACCCCTCT 2460
ACTTTGAACT TTTATTTCTC TGAATCATGA CAGCTCCCTT CAAAAAGGCA TTATCTCCAT 2520
TATTTTTAGA TAAATTTTCA TATGGTGACA TGTACAAATC TTAACTGTAT AATTTCATGA 2580
ATTAGGCCAG TGTAAATATC CATGTGACCA GTACCCTAAT AAAGATACAG AACATTTCTA 2640
TCACCACAGA AAGTCCCCTT GGGCTCTTTT CTAATTGGTC TCCACCCCAG GCAACCTCTG 2700
TTTTGTTTTT GTGTTTTTTT TTTTTTTTTA AGAGATAAAG TCTCGCTATG TTGCCCAGGC 2760
TGGTCTCGAA CTTCTGGGCT CAATTGATCC CCTGCCTCAG CTCCCACAGT GCTGGGATTA 2820
CAGACGTGGG CCACCACTCC TGGCCTTATT TTCTATTGAT ATAGATTAAT TTGCTTTTTT 2880
GAATAAATGA AATCATACAG TATGCATTTT TTTTATGTCT GGTTTCTTTT GCACATGTAA 2940
|
