| Tag | Content |
|---|
EnhancerAtlas ID | HS101-00642 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:21668790-21671860 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:21670116-21670137 | ATGAGGAAACTGAAACTCAAG | - | 6.21 |
|
| | Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
| SE_00105 | chr1:21656775-21671990 | Adipose_Nuclei | | SE_00854 | chr1:21667352-21672486 | Adrenal_Gland | | SE_01643 | chr1:21667344-21672121 | Aorta | | SE_02944 | chr1:21668309-21669287 | Bladder | | SE_02944 | chr1:21669307-21669834 | Bladder | | SE_02944 | chr1:21669946-21672098 | Bladder | | SE_03598 | chr1:21669025-21670171 | Brain_Angular_Gyrus | | SE_04518 | chr1:21668259-21672052 | Brain_Anterior_Caudate | | SE_05710 | chr1:21667990-21673560 | Brain_Cingulate_Gyrus | | SE_05944 | chr1:21659989-21673592 | Brain_Hippocampus_Middle | | SE_08398 | chr1:21667381-21673694 | Brain_Inferior_Temporal_Lobe | | SE_26127 | chr1:21667455-21671889 | Duodenum_Smooth_Muscle | | SE_26770 | chr1:21667319-21672743 | Esophagus | | SE_28486 | chr1:21667334-21672947 | Fetal_Intestine | | SE_29337 | chr1:21667313-21673152 | Fetal_Intestine_Large | | SE_31433 | chr1:21663236-21672659 | Gastric | | SE_39164 | chr1:21667486-21670213 | IMR90 | | SE_42174 | chr1:21667300-21672712 | Lung | | SE_44380 | chr1:21668279-21671929 | NHDF-Ad | | SE_45045 | chr1:21668251-21670150 | NHLF | | SE_46660 | chr1:21668354-21672080 | Ovary | | SE_47592 | chr1:21668748-21670086 | Pancreas | | SE_48583 | chr1:21667258-21672989 | Right_Atrium | | SE_50108 | chr1:21663357-21673470 | Sigmoid_Colon | | SE_52633 | chr1:21667302-21672599 | Small_Intestine | | SE_53334 | chr1:21667327-21672651 | Spleen | | SE_54639 | chr1:21663094-21674002 | Stomach_Smooth_Muscle | | SE_65263 | chr1:21660486-21671744 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGGAGGTTTG TGCCTGTTCT GGTACTATCT TGCTCTGTGA CCCTGGGCAA CCTCCTTCAC 60
CTCTCTGTGC CTGCTGCAGG GTGGTTTGAG TACAACCGGA GGCAGGAGAC ATAAAAAGCC 120
TCCTCAGAAC CCTCGGCCCA CGGCTTGCAC TGGGAGAAAA CAGGGGGAGA CGGTCCATCC 180
GAGGCCCTTA AGAACAGCAC TGACTCCCTG CCAAGGGGTT AGAGACGTGG GTGGGGAGCT 240
GGTGACCATC AGGGAGATTC AGTGAGGACA ACAGGAAACA CATCACACAG ACACACAGAC 300
ACACACAGAT ACACACACAC ACACACACAC ACACACACAC ACACACACAC GCCCTGCAAA 360
CGCGCCGCAT TAGGAACCCA GGGGCCAAGG ACAACTTGGC CACACTGCAA AGAAGTGAGT 420
GCTGGATTTG TTTAAAAGCC GCGGAGCAGG AGATCCAGGG AATAAACACT TGATCAGTCC 480
CGAATCACCC CTGCCTCAGG AATGACAGCA CAGGAACCAA TGTTTAGAGG AAATTAAAAT 540
GACAGGAGCC AGGGAGGCCT GACATCAGCC GCCACCCCAT GCATGCACCG CCGGTCAACA 600
ATCCACCGTG GACTTCCTCA GCCTAGTACT TTCTGGCCCC AGCAACCTTT TTGCCCTCTT 660
TCTCTTTTGT TTCCTGACCC TTTCATAGCC AGGTGCCAGA CCAGCCCCAT TCTGGCCTTT 720
CCAGGAGCCT GTCCTGTGCA CTCACACCTC TGCTCCTCTG TCACACAGGT CCCCCTCCCG 780
GGACACCCCT TCCAGTTCAG ATGTCACCTG CTCCATGAAG CTTTCTCTCG TCTCTCCAGC 840
TTGGAGAGAG CCCCTGCCTG GCATATTTCT ACCTCTCCAA GGACGTGCCA AAAAGTCTGA 900
GGACCAGTGC AGACGTTTAT GGCCTGGTGG AAGCTCCCAT AACACTGTTT ATTCAGTCAA 960
TTCTTTCCTC CCTCACATGG GGTTTGGCTT AGAGTAAGTG TTCAACACGT CCTGGCTAAA 1020
TGACAGACGA AAGTATCACG GTCTCCTCCC TACAACATGA TAAACTTTCA TTCGTCTTCC 1080
AGACCAGCAA ATAGGTGGCC TCTGTCCCTG TGCTGGAAAA GCCAGCCCAT AGCCCTGGAC 1140
AGATGGATGA CAGACTTTTG TTTTGGATTC CAGAGACAAC CCCTGGGGCA AATAGGTTAG 1200
ATGTTAGGTA GAACTTCCCA GCGTGGGCTC AAGCTTGGAA AAGAAAACTA AGCAGTACTG 1260
AAGCAAAGCA CTCTCACTTG GGTTATCTCA CCCTTTGGAG GTAAGTGTTA TCATCTCATC 1320
TTGCAGATGA GGAAACTGAA ACTCAAGGGT GATGCTTCAC CTAGACCAAA GTCCCTGTGG 1380
GGAAGTGGAG GGGATGGGGT TCAAACACAA ATTGGTGTGA CGTCAAAGCC TGGACTCTTC 1440
ACAATAGGCT GGTGGGCTTC TTCAGTTGTA AGGATCTATA AAGTGTCACC AAGGCAAAGT 1500
GAGGGGACCT CTTTCTTTTT TTGGTGGTTT TTAAGGAAGA AAAAATTTTC TTTATGAGTA 1560
ACTCAGGGTG GGCTTAGAGG CAGAGGGGAT CATACAACCT CAAAGTCTCA CGGCCTTTTG 1620
GTGCCCATAC ACTGAGACTT TAAATCCAGT GCTGGTCCAC AGATAGTGCA CTCCCTGTGT 1680
CGGAAACGGT CTGGGTGGGG CATTACAGGG GAGATTCCTA ATGGAGGAGG TAGGTTGAGT 1740
CTCACGTGGT CTCTAAGCAC CTTCAGGTAT AGAACTAAGC CATAATTCCA CCACTTCTGA 1800
CTCTAGTGAG GCAACTGGCG GTGCCTAAGC AAAGAAGACC CTAGCTGGGT GAGAAGAGGC 1860
CTTGGAAGGG AGAGATGGGG GGGCGGGTTG TAAGGGGACT CCAGCTCTGG GCACAGCAGG 1920
GGCTGGGAAC CACTGTGGGA CTCTTCGGCT TTACAGGGGG TCCCATCCTG CTCCCATCCA 1980
GGCGCCCTCG GGCTTGGCAG CATCATCACA GAGAAGTGGA GGGGCTGGAT CACAGGTACT 2040
GGCAGCCACC ATCCCAGGCA CATGCCCTCC TCAGCCCTAC ATGGTGACTT TGACCCACTT 2100
CACAGGGCAC AGAACAGAAC TAGGAGAGGG AATCCGAGTG GCTCGTCTAT AGGGAAAGAA 2160
ACCAAAGAGA AGTAGATGGC TCCCTTCCCG TGATGGAGAG GCCGGCACCC GGCCCTGGAC 2220
AAGTGGACAA AGGGCCTTTG CTCTTGGGGT CCAGGGACAA TGCCCCTCCC AACAGCCCCC 2280
CCCCAGGAAG CCCAGCCTGG ATCAAATGGA TTTCTCTTCT GGGGCTTTAG AGAGCCCCAT 2340
GAAACGCCCC TCCCCAGTTC CCTTTCTCCC TGGTACTCCT GCCTATCGCA GTCAGCACTC 2400
GGCCTCAGCA AGCCCCTCCT CTGAGGACCC ATCACCGGGA GATGCTGGGG AGACCGGATC 2460
GCTGGGTGCA GGGCCCCTGA GTGTCCCCTG GTCTCTGACA GCACCGACCT AGCTGCGTCG 2520
CCACCACATA CACCCCTTAG GCCACAGCTG GATCAGCAGT CCCAGAGGGC CGCAACCTAG 2580
CCCTCCGAAT GCGCCGGGCG TGGCCACCCA CAGTGCCCCA AGGCGAGCCC CAGACCGACC 2640
TCAGTGTCCC GGGACGCTCA GGTCCAGCTG CATCCAGGCA CCTCGAAATC GCCGCCACCC 2700
GCGAGCCCGA CCCAGCCCGG CTGCCCTGGG TCTCCAAGCC AAGCTGAGTC CAGGGACTTC 2760
AGAACAACCC AAAACAGACC GCAGCAACCG TCCCCAAAGC GAACCGGGGA CCCCGAGCCC 2820
CCCACATCCG GCTGGGACCA GAACCAAGCT CGGCGCGGCC GCCCCCGACG GGACCAAGCG 2880
CAGCGCCGCC GGGAGAGCCG CGCTCTGCCC GGGCGCTCCC CGACTCCACG CCTTCCGAGA 2940
GCCGGGCGGG GGCTGCTGCT GCAGCCGGCG CCCAGCCCCC CGCGAGCCAG GGCGGCCCCG 3000
GGTGCCACCC GCGGCACCGC TGCCCGCGAC CGTCGAGGCT GGGCTGGACC GGACCAGACC 3060
TCCGCGCGCA 3070
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