| Tag | Content |
|---|
EnhancerAtlas ID | HS034-18007 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr2:232535570-232537010 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr2:232536651-232536662 | AGCCACACCCA | + | 6.14 |
|
| | Number of super-enhancer constituents: 41 | ID | Coordinate | Tissue/cell |
| SE_03344 | chr2:232536403-232537111 | Brain_Angular_Gyrus | | SE_03959 | chr2:232535810-232538573 | Brain_Anterior_Caudate | | SE_05028 | chr2:232535737-232541459 | Brain_Cingulate_Gyrus | | SE_05842 | chr2:232525855-232541886 | Brain_Hippocampus_Middle | | SE_06810 | chr2:232535823-232540519 | Brain_Hippocampus_Middle_150 | | SE_08041 | chr2:232535600-232541750 | Brain_Inferior_Temporal_Lobe | | SE_08891 | chr2:232536445-232536692 | Brain_Mid_Frontal_Lobe | | SE_10218 | chr2:232534383-232541303 | CD19_Primary | | SE_11120 | chr2:232525439-232541839 | CD20 | | SE_23069 | chr2:232535541-232540349 | Colon_Crypt_1 | | SE_23744 | chr2:232535553-232537095 | Colon_Crypt_2 | | SE_24686 | chr2:232535534-232540308 | Colon_Crypt_3 | | SE_26538 | chr2:232535517-232540238 | Esophagus | | SE_27945 | chr2:232535465-232540390 | Fetal_Intestine | | SE_28950 | chr2:232534877-232540439 | Fetal_Intestine_Large | | SE_30147 | chr2:232535656-232538615 | Fetal_Muscle | | SE_31275 | chr2:232535767-232538558 | Fetal_Thymus | | SE_31583 | chr2:232535516-232540282 | Gastric | | SE_32771 | chr2:232535630-232538405 | H1 | | SE_34301 | chr2:232534523-232540475 | HCT-116 | | SE_34676 | chr2:232534862-232540487 | HeLa | | SE_40924 | chr2:232534079-232540431 | Left_Ventricle | | SE_42371 | chr2:232535488-232540392 | Lung | | SE_48427 | chr2:232535488-232540315 | Psoas_Muscle | | SE_48956 | chr2:232535490-232539914 | Right_Atrium | | SE_50073 | chr2:232532989-232540415 | Sigmoid_Colon | | SE_51193 | chr2:232536444-232540498 | Skeletal_Muscle | | SE_52583 | chr2:232535520-232540394 | Small_Intestine | | SE_53812 | chr2:232535508-232540417 | Spleen | | SE_54893 | chr2:232535506-232540365 | Stomach_Smooth_Muscle | | SE_55415 | chr2:232535978-232536756 | Thymus | | SE_56815 | chr2:232535537-232538596 | VACO_400 | | SE_57994 | chr2:232535546-232537081 | VACO_9m | | SE_58398 | chr2:232468621-232552645 | Ly1 | | SE_60442 | chr2:232526263-232553020 | DHL6 | | SE_61093 | chr2:232461681-232552859 | HBL1 | | SE_61422 | chr2:232466061-232552901 | Toledo | | SE_62587 | chr2:232525960-232546908 | Tonsil | | SE_65285 | chr2:232534824-232540241 | Pancreatic_islets | | SE_66935 | chr2:232535485-232540479 | H2171 | | SE_68691 | chr2:232535291-232540184 | 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 |
| GH02I231669 | chr2 | 232534477 | 232541408 |
|
Enhancer Sequence | AAGTGCTGGG ATTACAGGCG TGAGCCACCA CGCCCGGCCA CACAGGTTGC AGATTTGATG 60
AAGGGCAGGG AGGAGGCTCT GGCTAAGACC AGGCTGGATC TGAACTTGTA GTCCAAAGGC 120
AGAAGGAGTG AGATCCAGAC TATCCCAGGA AGGAACTGGG GCCTCTGGAA AACCAGAGAG 180
GTTTTCCTCC CCTGAAGGGG TTTTGTGGCA CCGTCCCTCA ACAGGCCACC TGGTGGCCAC 240
AGAGGCTCAG GCAGGGTTGG GTGGGGGGGA ATGGGAGGGG ATGGGGTGGG TCAGGGCCAT 300
TGCTCCCTGC TGAGTCCCAC TGGGGATCAT TGTGACAGAG AGGAAACCCC TGTTGGTGCA 360
GGGAAGCCAA AGGAAAATAA AATTTGCCCC ACCCTGAAAA GGAAAGGAAG ACTCAGGAGA 420
GAGGCCCCAG AGGGGGAGGC GTTACTGCCC AAAGGCTCCC AAGACCTGTC AGGTCAGCAG 480
ACACCAGCTG TGTCCCAGCA GAAGGTGGCC GGTTGAGCCC AGCTCCAGGA GGACACCAGC 540
TCGGCTCCCA TGCCACAAGG GCTGGTCGGG CCTGAGAAAG CGCCTGCCCA GATGTGCCAA 600
GGAGAGTTGG CCCCACACCC AGACCTGCAC TGCTGACTCC AAGCAGAGGC TGCGCCCACC 660
TCACCCTCCT TCCTGCAGGA AGTGTGGCTT TGCAACAGTG GCTGGTCTGA GGAACTGCCT 720
CCTAGGCTAA GCCCTCTGGC TACCTCCCCA GGCCTCAGGG ATCCCCCTGG AACACACCTG 780
CAGTCCCGTC CAAGGCAGGC TGTGTACTCT GAAAGAGCCC TGGGGTTCCA GGACAGAGCC 840
CACCGGCGCT CACTGGCTAG AGAGCCTGGG GCAGTTCACT CTGCCAGCCG GCCCCCAGTG 900
CTCAGTCCCA GCTCTGCCAG CCAGCATGTA ATTTTTCTGC CTGTGAGAGC GTGAGCCACC 960
TGAGCCGGCT GAGCTGAGTG GGCAGGACCA GAGGTCAGGA CCAGAGCCTG GGTGCAAAAT 1020
GCAAACATGG CCCCGTATGC AAATCACTCA GTTGTTTGTT CCTTCTCTCC TGACAAGGGC 1080
CAGCCACACC CAGATGCCGA AAAGAGCGCG CATGGCCTGG TCCCTGGGTG TCCTCAAGAG 1140
AGGAGTGGGC TGGGCACCTG ATGGAGCACA GCAGCGCTAA CCTCTGGGGC AGGACCCAGC 1200
TGAGCAGACG GCCCTTTCTC TTCGGAGCCG CGAGCCCTCG GTCTCCGCCC GAGGGAATTC 1260
ATAGCATTCT GCCTTTCCTG AAATCACTCC TGTCCCAAGT GGAGTCATCC CACAGACCAT 1320
CAGTGATGTC TGTTTCCCCA GGCTCAGGGC AGACTTTCAG TCTGGGGCTG AGGTGGCCCT 1380
GTGTGTCTAG GGGCTGATGT GGGCAGACCT TTGAGGAGCT GGCTGGGAAC CCCTCCCCCG 1440
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