| Tag | Content |
|---|
EnhancerAtlas ID | HS095-25391 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr6:3376860-3379480 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP2 | MA0593.1 | chr6:3377371-3377382 | TTTGTTTACAT | - | 6.14 | | GATA2 | MA0036.3 | chr6:3378738-3378749 | TTCTTATCTGT | + | 6.14 | | Gata1 | MA0035.3 | chr6:3378738-3378749 | TTCTTATCTGT | + | 6.62 | | NR2C2 | MA0504.1 | chr6:3378492-3378507 | AGAGGTCAGAAGTCA | + | 6.18 |
|
| | Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
| SE_03267 | chr6:3376379-3377157 | Brain_Angular_Gyrus | | SE_03267 | chr6:3377218-3377976 | Brain_Angular_Gyrus | | SE_03899 | chr6:3371888-3378737 | Brain_Anterior_Caudate | | SE_03899 | chr6:3379206-3395338 | Brain_Anterior_Caudate | | SE_04816 | chr6:3371075-3396288 | Brain_Cingulate_Gyrus | | SE_05855 | chr6:3371534-3378870 | Brain_Hippocampus_Middle | | SE_05855 | chr6:3378957-3396032 | Brain_Hippocampus_Middle | | SE_06865 | chr6:3372236-3378638 | Brain_Hippocampus_Middle_150 | | SE_07816 | chr6:3371641-3378755 | Brain_Inferior_Temporal_Lobe | | SE_07816 | chr6:3379158-3395583 | Brain_Inferior_Temporal_Lobe | | SE_23195 | chr6:3377342-3378802 | Colon_Crypt_1 | | SE_23990 | chr6:3377445-3377900 | Colon_Crypt_2 | | SE_26116 | chr6:3376444-3377892 | Duodenum_Smooth_Muscle | | SE_26690 | chr6:3377293-3378973 | Esophagus | | SE_26690 | chr6:3379093-3379875 | Esophagus | | SE_27773 | chr6:3377202-3378861 | Fetal_Intestine | | SE_28645 | chr6:3377119-3379036 | Fetal_Intestine_Large | | SE_31490 | chr6:3376946-3378858 | Gastric | | SE_31490 | chr6:3379101-3380631 | Gastric | | SE_36694 | chr6:3376990-3379212 | HMEC | | SE_42040 | chr6:3376344-3377422 | LNCaP | | SE_42040 | chr6:3377484-3378363 | LNCaP | | SE_42040 | chr6:3379101-3380483 | LNCaP | | SE_50390 | chr6:3376262-3378598 | Sigmoid_Colon |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 5 | Chromosome | Start | End |
| chr6 | 3377484 | 3378910 | | chr6 | 3377189 | 3377387 | | chr6 | 3379034 | 3379381 | | chr6 | 3377189 | 3377509 | | chr6 | 3377724 | 3378098 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH06I003376 | chr6 | 3376341 | 3377157 | | GH06I003377 | chr6 | 3377268 | 3386183 |
|
Enhancer Sequence | CCTTACATCA TTCGCTTATT TTACAAGCAT TTCATTCAGT GTATTTAGGC ACAGTTCACT 60
GTATTAGGTC ATTTGGACAA AAATGGACAG GACAGACAAT TATCTCGTAG ACTAGCTGGA 120
GTGAGAAGGC ATCCTGTAAG AAAGGCAAAA GTGAAGTAGG TCCTGCAGGG GTTTGGGGAG 180
TGAGGCTGGC CTCCTGGCTG GGAGGGTGGG GGAGATGGGA AGAAGATCTT TCAAGAAAAA 240
GGGCCTTCTG AGTTGGTCCC TGAGAAACAG ATAGAATGTG GCTATGCAAA TGGTAGATGG 300
AGGAAGAAGG GCATTTCAGA TGGAGGAGAG GGTCCACATG AAGGTGTCGG GGGAAGGGCT 360
GGGTGGAGAG CTCCAATTCT GATCTAGTAG CAATATTGTC CTTACTTCCA ATCAGGTGAG 420
TCATCTAGAG CAGAGGTTGG CAAACTGCAG CCTGCGGGAC AAATTTGGCC CACTGCCTGT 480
TTTTGTAAAT AAAGCTTTAT TGTAACACCC ATTTGTTTAC ATATCATCTG TGGCTGCCTT 540
ATGCTATGGT GACAGGATTA AGTAGTTGTG ACAAAAAACA TATGGCCTGC AAAGCCCAAA 600
ATATTTACCA TCTGGGACAT TACAGAAAAA GTTTGCTGAG CCCTAGTCTA GTATTATAGC 660
CAGGGAAGGT GTAGGGAGGA AAGGGCTCTT GGCCAAAGAA GGGCATTGCT GCTGATTACT 720
GATGGAATGA TGGAATGGAG AGGGTCAACA GAGGGAACAC TGGATGGAAA GCAGTGGGAT 780
GAATGCTAAG AGAGCCCACC AACTGCCAGA CCTCTGCCAG GCCTCCTGGA CCCTCTGGCA 840
GGGGAGGCCA CCCTGCTGTG CCTGAATGGT GCAGTGACTG GGTGCCACGT GTGTGCTCTC 900
TCCAGTCTGT GGGCAGCATG AAGGCAGAAA GCACCATTAT GGCTTTAATG CCTTCCCCTC 960
CCATGCAGCT GCATCCACAG GACCTGAGGA GTAAACTGTG CCCCTCCAAG TCTCGCACTG 1020
AACGTGTCTA GGCTGCAGAT CAGTGATCTC AGGCTGTACT AAAGAAAGAC AATGAGCAGT 1080
GGAGAACAGC ACTGGGCCAG GCAGAGGCTG TAGGTGGGGA AACGAGTGAG GAGACTATTG 1140
ACAACATCCC AAGATGGAAT GACACTAGCA CAGTGGCCCT GGCAGGGAAG TACTTACACC 1200
TCATACAGGC AGTCTCAGCT CCTCCAGAGA ACAGCCGCTG CAGAGGGGAT CGTGCCCCTT 1260
CCACTGCCCA GCAGCCACCA AAAGAACAAC AGGGCACTTG AGGTATCAGC AGTTCTGCCA 1320
GCCTGAGGAT GTTGCTGTTT CACAGCTCCT GGGAGCAATT CCTCCAGGGA ACAGGACACC 1380
CAGGAGTCCC GAGGTGTCTG CTGGGCAGGG CAATGGTTGT TATGGAATCT GTTTACCCGG 1440
AAACCACCAC GACGCCACAT ACCTAAGAAT ACCTAGGGCA CTTATGACTG ATTCCTACAT 1500
GCCCGCAACT CCTCTTTAAC ATTTAATATC ACCGATGGCT CCGAACACTT TGTACTTTTT 1560
GCTCAGCTGA CCTGGAAGCC TTTGGTCGTT TTCCCTCCTA GCTGGGCCCA TGTTTGTCAG 1620
GTGGGTGCAC TGAGAGGTCA GAAGTCAACA TGGCCCGAAG TCCATCAGGC ATGGGTGGTG 1680
AGAACCAGGA CCGTTCTCCC AGGAATAGAA GGGTGAAAGC ACCTGCAGAC CTCGGCCCGT 1740
GATTCAGCAC TTACTCCTGA AAGACTTGAG GGTATTTTTA AAACTTTTTA CAAAGCGACC 1800
ATTGCTGCTG TTGCTACTGA GGCAACAGGG TAATTGTTTC CTTTGAAAAG CCATCACTTC 1860
CTCTCCTATT TTATGTGGTT CTTATCTGTC GACTGTGACT GGCTTTCACT ACTTGAAGGG 1920
CATTAGACTG GAAGTCTAAG TTCTCACCCT GGCTCAGATA CCATCTGTCC AGCCTTAGAT 1980
ATGCCTCTGA ACCTCTCTCT GTGTCAGACT TTTTTTTTCT TTTCTTTTTT CTTTTTTTTT 2040
TTTTTTTTGA GATGGAGTTT TGCTCTTGTT GCCCAGGCTG GAGTGCAATG GCGTGATCTC 2100
GGCTCACTGC AACCTCCGCC TCCAGGGTTC AAGCGATTCT CTTGCCTCAG CCTCCTGAGT 2160
AGCTGGGATT ACAGGCACCT GCCACCACAC CCGGCTAATT TTTTGTATTT TTAGTAGAGA 2220
TGGGGTTTCA CCATGTTGGC CAGGCTGGTC TTGAACTCCT GATCTCAGGT GATCCACCTG 2280
CCTCAGCCTC CCAAAGTGCT GGGATTACAG GCTTGAGCCA CCGCGCCTGG CCTCAGTGTC 2340
AGGTTTTAAC ATGAAGGAGG AGCTGAATCG TGGCCTGGGC TCTAAGTTGC AGGTCAGGCA 2400
AAACCTGTCT TTATGGGAGA GTTGTCTGGG CCTCCCTGCC AGCATGACAC TTTTTGCCCT 2460
GTTTTCTCCA CAGTGTAATT CTGGTGCCCT TAATGAGCTC TCTGGAGATT CTCTCCCATG 2520
GCTGGCCTGT CTCTGAGACA AGTTCTAGTC TCTGATGTTG AGTCTAGACC ACAGCAACAA 2580
TTCTAAAATG TCCTTCTCCT CCACCAAGGG GACTTCGGCT 2620
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