| Tag | Content |
|---|
EnhancerAtlas ID | HS129-08099 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr12:6290840-6293560 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP1 | MA0079.4 | chr12:6291837-6291852 | AGAGGGCGTGGCCTG | - | 6.15 |
|
| | Number of super-enhancer constituents: 36 | ID | Coordinate | Tissue/cell |
| SE_00985 | chr12:6290507-6292062 | Adrenal_Gland | | SE_00985 | chr12:6292206-6292982 | Adrenal_Gland | | SE_01613 | chr12:6290594-6292119 | Aorta | | SE_01613 | chr12:6292178-6293897 | Aorta | | SE_03988 | chr12:6290792-6291792 | Brain_Anterior_Caudate | | SE_04905 | chr12:6289324-6293306 | Brain_Cingulate_Gyrus | | SE_05857 | chr12:6287388-6293430 | Brain_Hippocampus_Middle | | SE_07876 | chr12:6289745-6293464 | Brain_Inferior_Temporal_Lobe | | SE_23086 | chr12:6290753-6292057 | Colon_Crypt_1 | | SE_23086 | chr12:6292201-6293938 | Colon_Crypt_1 | | SE_23760 | chr12:6290811-6292000 | Colon_Crypt_2 | | SE_23760 | chr12:6292242-6293084 | Colon_Crypt_2 | | SE_23760 | chr12:6293275-6293833 | Colon_Crypt_2 | | SE_24754 | chr12:6291005-6292084 | Colon_Crypt_3 | | SE_24754 | chr12:6292220-6293863 | Colon_Crypt_3 | | SE_25881 | chr12:6290586-6291938 | Duodenum_Smooth_Muscle | | SE_25881 | chr12:6292265-6293935 | Duodenum_Smooth_Muscle | | SE_26531 | chr12:6290619-6292172 | Esophagus | | SE_26531 | chr12:6292175-6293815 | Esophagus | | SE_27879 | chr12:6290695-6293924 | Fetal_Intestine | | SE_28805 | chr12:6290511-6293953 | Fetal_Intestine_Large | | SE_30052 | chr12:6290681-6292144 | Fetal_Muscle | | SE_31631 | chr12:6290651-6293026 | Gastric | | SE_34881 | chr12:6288010-6291925 | HeLa | | SE_37709 | chr12:6286475-6292578 | HSMMtube | | SE_37940 | chr12:6286549-6293824 | HUVEC | | SE_41013 | chr12:6288021-6292951 | Left_Ventricle | | SE_42122 | chr12:6287877-6292200 | Lung | | SE_42122 | chr12:6292204-6293894 | Lung | | SE_48662 | chr12:6287969-6292096 | Right_Atrium | | SE_50072 | chr12:6290476-6292094 | Sigmoid_Colon | | SE_50072 | chr12:6292172-6294061 | Sigmoid_Colon | | SE_52457 | chr12:6287948-6292107 | Small_Intestine | | SE_52457 | chr12:6292166-6294018 | Small_Intestine | | SE_53862 | chr12:6287321-6293849 | Spleen | | SE_54512 | chr12:6288437-6293993 | Stomach_Smooth_Muscle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 6292247 | 6292800 | | chr12 | 6291358 | 6291755 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I006177 | chr12 | 6286985 | 6293820 |
|
Enhancer Sequence | CTCAAGGAAC GTCTAGTCCA GGATTAGAAG TGGGGCAGTC CCAGGAAGGA GCCATCTTGA 60
CAGTGAATTC ACGCGGAAGA CGCGTGAACC CAGCTGGCCT GGAGAGACAG AGGTGCTTTG 120
CAGGGCATGG GGAAGCCAGC AGGTCCCAGT CGAGAAACCT GGTTTTCTGT CTGGGTTGGT 180
TGAAGACTCT TTGTCCCAGA AGGAGTCGCT TGTTTGCTTG TTCATCTTAA GTTTAAATTG 240
AGAGAGGTTA ACGGCTTTTG CCTCAGAAGG CAGGCTGGCC TGGCAGGGTG TGTGTTGTGA 300
GGTGCAGAAA CACATCTTCC CCAGCTGGCC TCACAGGCCA AGAAGCAGAT AATGTCTTCC 360
TTCTGCCAGC TTCCCCGCAG CTTGGTTTTC CTGGGACAGT TCCTCCGCTG GAGGAAGGGA 420
CAGGGGATGG GGACAGGGGA TGGAGGAGGA GTTGGGGAGA CCCTTCAGAG AGTGTGGCAG 480
AAACACGTGT GTACAGGCTG GCACACGAGT CACAGAGGCA ACAGGGTGGC TGCGGGGAGA 540
AATGTGAGCA GAGCTCATGC AATTGTCGTG AGTGAGTGCG CTCTCGCGGC TCTAAGGATT 600
TGGGAAAACA ACTTGCAGAT CCAGGCATGT TTACGTAGGG AGGGGTGCCG TGTGCTGGAC 660
CAGGTCCAGA ACTAAAAATA ACACAGTATT TCTGTGCCCA GCAAGAGCGC TAGCATCTGT 720
GGGGTTTGCG TGGTGGGAAG AGTGTGGTTT CAGCTGAACC AGGCGCAGTG TGACCAGAAC 780
AGTAGGAGGG AAGGCCAGGC CTGGGTGGGA GGCCCCAGGA TGGGCGGGGG AAGGACTGAG 840
GGCGAAGGCC ATCCCAACTC GCAGCAGAAA AAGCCTCCAG GCGGTCACGG GCTGCCCATC 900
TCGTGAGGCC AGATGTGGGT CCTCCTGCAT ATCTGAAACA GCACAGAGCA TTGGGGCAGC 960
CTCCAAACCT CCCCTATAAG GAGCAGTTAA GGGATCCAGA GGGCGTGGCC TGGAGCAGAG 1020
AGAAGGGAAG CAACATGTGT GGGGCATTCA CAAGTGCAGG ATGCCTTCTC CGGGCTCCCA 1080
TGATGATCCA GACAGGTAGG CGTTTTCCTT CCCTTTTTGC AGATTGTGAA AACAGCGTTC 1140
AAAAAAGACT CATGGGCCGG GCGCGGTGGA TCACGCCTGT AATCCCAGCA CTTTGGGAGG 1200
CCAAGGCAGG CAGATCACAA GGCCAGGAGT TGAAGACCAA CCTGGCCAAC ATGATGAAAC 1260
CCTGTCTCTA CTAAAAATAC AAAAATTAGC CGGACGTGAT GGTGGGCACC TGTAATCCCA 1320
GCTACTCAGG AGGCTGAGGC AGGAGAATCG CTTGAAACCG GAAGGCAGAG GTTGCAGTGA 1380
GCCGAGATTG CGCCACTGCA CTCCAGCCTG GTCAATAAGA GTGAAACTCT GTCTCAAAAA 1440
CAAACCAACC AACAAACCAA AAACTCTTGT AACCCTGGGG CCACCCAGCC ACAAAGAGGC 1500
AGGGCTGGGA CAGGCCCCTG CAAGTCTCCT CTGGAAGGCC AAAGGGCTGC TACTAGGAAG 1560
GGGTGGCAGA CTCATCCCAT GTGGCTTCAG AGGGCAGGAC ATGGACAAAG GTTATGGGAA 1620
GGGAGGGAAA CTTTCCAATA ACCAGACTGC ACAAGAGTGG AGTGGCCTGC CTCAGGAGGG 1680
GTAAGCTCAT GCAAAAGCTG GCTGTTGGGG ACATTGGGAG GGACTCTGAA GGTCACCACC 1740
ACTCTGAATC AATGCTGTGT GGGAGGATGC CAGGGTCCAC TGGACCCATG ACGTGCCTTT 1800
AGCGTGGGAA GCAGGGAACC TCAACTTTGG AAAGAGTGAG GGCACAGTGA TGTCCAGCCA 1860
CTCCCAGAAG CCGTCTGTTA ATAGAGCAAC CCCTCGGGCG GTGTGCAATC CTAATGACCA 1920
GCCCCAGGAC ATTGGAAACA GGGTCCTGCT GACCACAGTC TAGGAGACAG GGCTGCACAC 1980
AGACGGAACC AAGCACACAA GACGAGAGAG GGTGTGTACC GCAGAAACCA AGGGCTCATT 2040
TATGTGCTGC GTTCTCAGTC TGCAAGGAGT CAGAAGAGAG GACAGTGAGG CCAGGAGAAC 2100
TCAGGGAACA CTCCTTGTTG TAATCATCAC AGTTATGTAA CTCATATTAC CAGCTGTTCT 2160
TTCGTGAGCA TTCTCTATGT GCCAGGCTAA GTGTTTTGTA TGCACTGTAT GATTTAATCC 2220
TAGAACAACA CTATGAAGCA GGAGCTCTTA GTATTCCCCT TTTACAGATG AGGAGGCAGG 2280
CTCAGAGAGG TGATGTAACT TGCCCAGAAT TATATAACTA GTGTGTGGCA GAGCCTGGAC 2340
TCAAGCCCAG ATCTGTTGGA CTCCAGACCC CGTGTAGAAC CATAAGGAAC TGATGCTGCT 2400
TCAATTTCTG CACTGATACG GAAATCTCTC CGAGATATCA TGCCGTTGTT TTCTATTGTT 2460
GCTATAGCAT ATTATCACAA GTTTAACACA TATTTATTGC ACACTTCTGG AGGTCAGCAG 2520
TCTGACATGT GGGTCTCACT GGGCTAAAAT CTCAGTGTGG GCAGGGCTGT GTTCCCCTCT 2580
GGAGGCTGCA GGGGAGAATC CCTTTCCTTG CCTTTCCCAG CTTCTAGAGG CTGCCTGCAT 2640
TCCTTGGCTC CTGGCCCCTC CTCTGTCTGC AAAGCCACCA TTGTCATGTC TCTCTAACCC 2700
TTTGTCCCAG TTCCCTCTGA 2720
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