| Tag | Content |
|---|
EnhancerAtlas ID | HS095-02685 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:204071390-204074370 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr1:204073699-204073713 | ATTCCCCTGGGACT | - | 6.33 | | EBF1 | MA0154.3 | chr1:204073699-204073713 | ATTCCCCTGGGACT | + | 7.17 | | FOSL2 | MA0478.1 | chr1:204073903-204073914 | CTGAGTCACCC | - | 6.02 | | IRF1 | MA0050.2 | chr1:204071935-204071956 | ATAGAGAAACTGAAACTTCCC | - | 6.17 | | IRF9 | MA0653.1 | chr1:204071937-204071952 | AGAGAAACTGAAACT | + | 6.28 | | JUNB | MA0490.1 | chr1:204073903-204073914 | CTGAGTCACCC | - | 6.02 | | KLF4 | MA0039.3 | chr1:204073569-204073580 | GCAGGGTGTGG | - | 6.62 | | ZNF263 | MA0528.1 | chr1:204071742-204071763 | GGAGCAGATGGAGGAGGAAGA | + | 6.48 | | ZNF263 | MA0528.1 | chr1:204071751-204071772 | GGAGGAGGAAGAGGGTGGCGG | + | 6.66 | | ZNF263 | MA0528.1 | chr1:204071748-204071769 | GATGGAGGAGGAAGAGGGTGG | + | 6.71 |
|
| | Number of super-enhancer constituents: 16 | ID | Coordinate | Tissue/cell |
| SE_01182 | chr1:204071129-204074607 | Adrenal_Gland | | SE_06365 | chr1:204070800-204074466 | Brain_Hippocampus_Middle | | SE_24644 | chr1:204072637-204073956 | Colon_Crypt_2 | | SE_29514 | chr1:204070868-204072610 | Fetal_Intestine_Large | | SE_31799 | chr1:204070890-204072352 | Gastric | | SE_31799 | chr1:204072461-204074581 | Gastric | | SE_34793 | chr1:204069193-204075827 | HeLa | | SE_42361 | chr1:204069421-204075729 | Lung | | SE_47675 | chr1:204073025-204073996 | Pancreas | | SE_49400 | chr1:204070904-204074543 | Right_Atrium | | SE_50648 | chr1:204070818-204074547 | Sigmoid_Colon | | SE_53078 | chr1:204070806-204074527 | Small_Intestine | | SE_54451 | chr1:204071112-204074613 | Spleen | | SE_65332 | chr1:204070923-204074836 | Pancreatic_islets | | SE_68685 | chr1:204070894-204072274 | H9 | | SE_68685 | chr1:204072447-204074590 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I204100 | chr1 | 204069922 | 204075641 |
|
Enhancer Sequence | TTGTCCTTTC CGCTGTCTGT AGTCATCCCT ATGGTCCCCA CCTTCCTCTC CCTCTGGGGT 60
TGGCAGGAGA ACGCAAGGGT TAATGATATA GCACTTCACC CTTGTGGGCT CCAGAGGAAA 120
TGAGGGAGCT CATGAGTTCT GCAGAGCTTT TGTGTCATCA GCCGGGGAAG GGAAGGCACC 180
GTGGCTTGGC CAGATAAGCG GTGGCGCTGC GAATGTGGGG CTTCCTTGGC AGATTTGTAG 240
CCTTTCCGCC TGTTTGCACT GTGGGGCACC TGCTGGGGCT TCCAGGGTGG TTGGGGACAT 300
CAACAGGGCA TTCAGAAAAC TGATAACCTA GGCTAGGGAG GGAGACCTAC ATGGAGCAGA 360
TGGAGGAGGA AGAGGGTGGC GGGCCCTGGT GTTCTGCAGG TGCATGTCTT CTGCTTGTTT 420
GACCATGTGG GGGAAGGGGG TGGCGGTGGG TCAGGGAGCA AACATTTTTT TGATTTTCAC 480
AAACACCATC ATATTCAGTC TTCTCTATCT CTATGGGGTA GGTGTTATTT GTTCCCATTT 540
TAGAGATAGA GAAACTGAAA CTTCCCCATG GCCACACATC TAGTGGTATA TAATAGAGCC 600
AGTCTTCAGA CACAGGTCCA TGTGACAAAG TCCTTTTTCC ATTAGCCACA CCAGGATGCC 660
TCCCAGCAAT GCTGGGTCAT CACACCCACC CACCTGCCTC CGGAAGAGCT GGGCTGGCTG 720
GGGAGGAGAA TAGGGTGTGA GTCCTTCTCC CCCTTGCCCT GGGGGCAGGG AGGGAGAGGG 780
ACTCCTTCCT GCTTTAGGGC TCTTTCTCCT TACCTCCTTC CCTGAACATA TATTCTGTAC 840
CAGATTCTGT AATTATACCT TATCTCTTAC TCACAAAATA GTTCTTGGAA TCTCTATTTT 900
ACACATGAAG AAATGGGGGT TTTGAGAGGT GAAGTCTTTC CCCCAACTTG CCAGAGCTGC 960
CTGGGTTTCT TTTGACTAAG TTTTCCTTGG CTATGACTCA AGTCAGAAAC AACTGCAATC 1020
CTGTAAGAGG TGAAGACAGT GGCCATTCTA TCTCTGCTGG ACCAGAGCCT GTTATTTTGC 1080
ACCGAGGAGA GTGGCCAGGG CATCAGCTGA TAAATGAAAG GATGTGGATT TAGACATCAG 1140
CGAGGCCTGA GTTCAAATGC TACTTCTGCT GGGCCCTCAG TAGGACGTTC TAGCCCCCGA 1200
GCCTTAGTCT TTGTAGTGTT CTTGTGAGGA TTAAGCAGGA ATGTGAATGA AGAGCCTTTC 1260
ACTTAGTGCT TGCAGCCAAG TAAGTGCTGT AGCATTGCAT GCTTGCTTTT TGCCTCCCAT 1320
TCCTTTGGTC AGTATTCAGG GCTATCCCCC AAGGGGCCTT TGACATGGCC AGTCAGCCTC 1380
AGCTGCACAA TTTCTGCATC TCCCAGCCCT AGGCTGGGCA CTGTCCCTGC AGGAAGCCAG 1440
ATGTGCTCAC CTGTCCAGGA CACAGGCTTG GCCTTGCCAT TGGGAAACAA GGATGAGGCC 1500
TACCCCTGCC TTCTAGCACT GTTGGGGTGC AGGAGAACCT GGAGACAGGC TTGGGTTCTA 1560
GAGGCAGGAA GGCCTCCAGA GAAGGGCCTC CTAGAGACAC TGTTGACCTC TTCTCGGTTT 1620
GGGACCTTCT GGAGGCACAC ATCACACTGG GAGCCTCAAT GGCGCTTTCA AGCAGTCCCA 1680
TCTGTCTCTT TCTCGACCCA CTCACTGGGT TGGGAGAAGA CTCAGGTGCC TCTGAGGCCT 1740
GAGGACCAGG TGGGAACATC ACAGCTACAG TCTCTCCCTG GCCACTGTTT TCCTTTGTGC 1800
CCTTGGGCCA GGGTCAGCTG AGTCCCGGCA GCCACAGAAG CTCAGGCTGG ACTGTGATTC 1860
TGTACCTGAG GTGCTGTGGG GAAGTGCCTC TTCTCCCATG CTTGGGAGTT GACCCAGCCT 1920
CTGTCTGATG TTGGCCACTC TACCAGGTGA ATGCCACCCT GACCAGCCTG GAAACAGCCG 1980
AGGGAGTGTT GGCTGTGGCC CCCCTGAGCT GGGCTAGACC AGACCGGCCG TGCCCTGGAT 2040
CTGATACCCC CCAGGGCTCA CAGAGGCTGG AAAGGGTGAG AGGGACTCGC AGGAAAGCTT 2100
TGTCCCAAGC CTGCAGCCAG TCCAGCTCCC AGCTCTGAGT AAACATTAGA GATAGGATCG 2160
GGTGTAGCCA GGAAGGGTGG CAGGGTGTGG TCTGTGAGAA GAATGGCAGG ATGTGGCACC 2220
GGGGCACTGT TCTGGGCACC CACGCCTTGG CCTATTGTTT AGGGCAGCCT GAGGTTCTCA 2280
GCTCTCTGGG GGCTTTCAGA GGAAGTGGCA TTCCCCTGGG ACTCAAGCCC TGCCCCACCC 2340
CTGCTGCATG GATCTCTTTC CCTGGTGATG CCCCTTGGCA CCACCCACTC AGAGCAAGCT 2400
TGGGAGTGGG AGCCAGCAGT GGAGGGGGAT TAGTGTGTGC CCAGCGGGGA AGTGTAGCCA 2460
TTGGCCCTCT CAGAGGGTCT GCCTGTCTGT TCAGGCTTCC TGTACCCCAG GGTCTGAGTC 2520
ACCCGTCATG CTACGATGAC TGGAATTTAT CTCTATCTTT ATCTTCATCT AGATATTTTT 2580
TGTAGGGTGG GGGAAGGCTG TCGTTGTGGA GGGAGGAAGG ACTGACAGTA AAAACTCCTT 2640
TGATTCCAAT CCAACAGGGT CAGTTGTTGA CTGGTTAGAA GAGGAAGTGG CTGGTGATTT 2700
GTTTTGGGCA GAAAGGGGCT AGGTTTGTGT GCGCCTGTGG GTTGGTGGGG TTCAGAGGGG 2760
CCGTGACAGG GCTGGTTGTG GGGAGGAGAG AGGAAGAGGA TCGGCACCTG CAGCGGGCTT 2820
TGTCATATAA GCGCCATGCT TTGAGCCACT GTCCCTCCAT GGAGGCGGGT GCCTCTCTAT 2880
ACCTTGTCTC AGGTGCTGGA TTTGGGGGCC TCGGGGCCTG GTAGGCACAA GCTGAGACTC 2940
AAGGCTCTGC ATGTCAAGGG CGAAGATGGC TGGAGCCCTC 2980
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