| Tag | Content |
|---|
EnhancerAtlas ID | HS083-00232 |
Organism | Homo sapiens |
Tissue/cell | HCC1954 |
Coordinate | chr1:202014730-202017470 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr1:202015499-202015511 | CTCTGTTTACAT | - | 6.32 | | FOXP2 | MA0593.1 | chr1:202015500-202015511 | TCTGTTTACAT | - | 6.02 | | IRF2 | MA0051.1 | chr1:202014977-202014995 | GGAAAATGAAACCTAAAG | + | 6.67 | | Znf423 | MA0116.1 | chr1:202015407-202015422 | GCCCCCCTGGGGTGT | - | 6.21 | | Znf423 | MA0116.1 | chr1:202015965-202015980 | GGCACCCTGGGTGGC | + | 6.36 | | Znf423 | MA0116.1 | chr1:202015965-202015980 | GGCACCCTGGGTGGC | - | 6.66 |
|
| | Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
| SE_23058 | chr1:202014631-202017594 | Colon_Crypt_1 | | SE_23723 | chr1:202014745-202017484 | Colon_Crypt_2 | | SE_24689 | chr1:202013412-202017599 | Colon_Crypt_3 | | SE_25977 | chr1:202013680-202018944 | Duodenum_Smooth_Muscle | | SE_26730 | chr1:202014480-202017654 | Esophagus | | SE_27624 | chr1:202013379-202018834 | Fetal_Intestine | | SE_28545 | chr1:202011166-202018857 | Fetal_Intestine_Large | | SE_31432 | chr1:202014570-202017653 | Gastric | | SE_33417 | chr1:202013470-202017710 | H2171 | | SE_33792 | chr1:202014660-202017539 | HCC1954 | | SE_34304 | chr1:202014463-202017386 | HCT-116 | | SE_34741 | chr1:202015302-202017356 | HeLa | | SE_41626 | chr1:202014836-202016985 | LNCaP | | SE_43434 | chr1:202014625-202017551 | MCF-7 | | SE_50066 | chr1:202013466-202017590 | Sigmoid_Colon | | SE_52354 | chr1:202013521-202017654 | Small_Intestine | | SE_56834 | chr1:202014865-202017504 | VACO_400 | | SE_57376 | chr1:202014892-202016968 | VACO_503 | | SE_57945 | chr1:202014917-202016359 | VACO_9m | | SE_57945 | chr1:202016368-202017040 | VACO_9m | | SE_65333 | chr1:202014451-202017286 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 202015600 | 202017009 | | chr1 | 202016172 | 202016526 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I202042 | chr1 | 202011209 | 202018712 |
|
Enhancer Sequence | ATCTGCCCAA TTCGGCTTCC CAAAGTGCTG GGATTACAGG TGTGAGCCAC TGCGCCTGGC 60
CAACTGCATG GAGTTTTTAA GATTTCCTAT GGCCCAAGTA CTCATAAGCA TCCTGCATGG 120
ATTAACCCTG AGAGGCAGGT GGTATTATTA TTCTCACTCT ACCTGGGTTC CCACCTGATA 180
ATTGGTGAGG CCCTTTCAAA TGTCCTTTGG CCTTCTATCC CCTGCCTTCT CTTGACTCCT 240
TGAAGTGGGA AAATGAAACC TAAAGTGCCT CCCTCCCCAG AGTGGGCCAT GTGGCGAACT 300
CTATCCAATG TCTCAGCACC TGCCACTCTC TAGTTGCATC CTGGCCATAG GCTGAATGGG 360
TAGGGAGTTC TCTGAGGCTG AGACCATGCT GTGAGGGAGG ATAGGCGGGC CAGGGACAGT 420
GCCAGCAACA GGGACCAGGG AGTGGTGGGA AGGTAAAATA AAGGCAGAGG AAACTTCTCC 480
CAATTGAGGC ACACCTACCC AAGGCCTCTG CCCCTACCCA GACTCCTGAC TTTGACCTGC 540
CTAAAATAAA TCCGGGGTCT GCAAATGGCC TGGAGGCTGC AAATGGCCTG AAGGCTAGTG 600
GTTGGAGGGC AAATAAAGGC AACTCATGGC ACTGCATGCT GCCCCTTGGT GGGCAGGTCC 660
CAGGTCCCAG GGTACCAGCC CCCCTGGGGT GTGATGTGGG CAGCCTCTGA GCTAAGTGAG 720
GTGCAAACAA GAAACCTGGG TTGCCTTTGC CCTCTGTCCG CCCCTTGTCC TCTGTTTACA 780
TCCTCCCTTC CCGTAAATGA GTTGGGTGCT GGGCCCCACT GGCCCTGATC CAGACACACC 840
TGTAGGACAG GTTGGGCAGA GCTCTTGGGG GTGGAGAGCG GGTGGCAGTA CTGGCAGGTG 900
TTTCAGGCCC TTGGGGAGCA AGCTCTGTTC CTTTCCATGG CAGTGCTGCT GCCAGGCTCT 960
TGCTGCCTTG GGCCAGGAAT TCTTGGCCAA CTCCAAAAGG ATGGGATGGC TCTAGGGGGG 1020
GCTACCTTGC CCAAGGAGTG CCAGGAAGTT GTGTTCAAGC CCTCAGAGGC AAGAGGACCA 1080
AAGGCTCTTT ATCTTCAGTG GGCATTTCCC AGCAGAAATC TGAGGTCTAG AGCGAGACAG 1140
AGTAGAATTG ACAATAAGAT CCACACTTGA GCTGCTAGCT GCCTTGATGG GAGACCCCAC 1200
TGTAACAAGA TGTCCAGGAG GAGGTGGCGG TACTGGGCAC CCTGGGTGGC TCTGCCTCTC 1260
TCTGGACTTT GTTCTGCAGT CAGGTCAGTT GAGGAAGCAA GAGTGAACCT GGAGTTTGGG 1320
TTTCTGGAAG GAGCAAGGGG GAAAGGCAGA CTTGGGCAAG GGACATAGGT GTCAGATGAG 1380
GCAAGTCTGA GTCAGAAGGC AGAGCCTGTG TCCCAGAGGA AGAGAAACAC CAGTGTCCAG 1440
CCTCCAGGCC ACTTGCAGCC CCCAGATTTA TTTTAGGCAG GTCAAAGTCA GGAGTCTGGG 1500
TAGGGGCAGA GGCCTTGGGT GGGTGTGTCT CAACTCAGAG AAGTTTCCTT TGCCACCAGA 1560
GGATTAACTG ACCAAGTTTA CCTAAGATGT GTTTTCCACC TGATCTCTTC TGTCTCTCTC 1620
AACAACAATG ATGACTGTGT ACTCAGTCAA CAAATATGTA GTAACTGCTT ACTATGTGCC 1680
CAGCCCTTTG CTGGGTGCTT AGATCACAGC TGTGTTCATT GGTGACTTTA CCAATCCATG 1740
GCATCATCTC GGTGGGGCAC TGTCCTGGTC AGCTCCTTCT CCCATTCCCT CCATCACTCC 1800
TCCACCCTCA CCTGCAGCTC CTGCATCTCT TGACTCTCAT CAAATGATCT TGCTGTCTTC 1860
TTCACGGGAA GGCCATGACC TCAAACAGGA AATCCTTCAG TTTCCCACCC TGCTGAATCT 1920
GTACCACCTT CCCTCCAGAG GAGTAGAAGA GGTGTCAACC CTGCCCCCGT GCTGGCGGTC 1980
CCAGTCCTGC TCAGCTTCTC TGGACAGGAG ATTAGCACAC AGAGGCTCAG CTCTAAGACC 2040
ACCTAGAGGC CTGCTTTAGG GGGTCCTGCT GAGTAAGGCA GAGGCTCAGG GTGGCCACAG 2100
TGGAGAACTG CTGGCTTAGC CTGCTTCCTG CATTGTGCCT GAGATGCCTG TGGCAAAGCT 2160
TTGCAGTCCC CACACCTGAT TCTGTATGTC CTGGGACACA ATGACTTGGA TTTCATCTTT 2220
TTTTTGTTTT TTCAAGCCAA AAATTAGGAT TCAGTTTATT CCAACATTGA ATGTATCAGG 2280
AAAACCAAAG ATAAAGTGAC AGAGGTACAT TAGGCACACT GTATACAGAT TTCATCTTTA 2340
CTTGACCTTT GCCAAAGAAC TATGCATATT CTGGTGATGG TGGTTTTCTT CAACAGATCT 2400
TTACGGGGAA GGCCCTCTCA TTTCCTCCAC ACCTTTCCTC TAGTGAAAGC GTTCTCAACC 2460
TCCAAGGAGT GTTGGGATTG TCTCCCCAGG TCATATCATC TGTCATCCAT ATGGGCTGTT 2520
AGCTCTGCGA TTTTTGTTCT CAGTCCCCAG GCTGTCTCTC AGCTCTAGAA GGAATTGTTC 2580
AAGGTCCTCC AGGTCCATGG CTCACTGCCT ACTGCCTTTT CCTTTTAGGG TGGTAAATTA 2640
TGGTAAAGTA AATATATGGG GAAACTAACA ATAGATAAGG ATTATTCAGG ATTTTTTTTG 2700
AAACAGGGTT TCACCTGTCA CCCAGGCTGG AGTGCAGTGG 2740
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