EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS117-04074 
Organism
Homo sapiens 
Tissue/cell
LHCN-M2 
Coordinate
chr2:218784950-218786560 
Target genes
Number: 3             
NameEnsembl ID
TF binding sites/motifs
Number: 12             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr2:218785691-218785712GGGGGAGAGTAGAGGGGAGGG+6.09
ZNF263MA0528.1chr2:218785739-218785760GAGGGAGCGAGAGGGAGGAGG+6.23
ZNF263MA0528.1chr2:218785749-218785770GAGGGAGGAGGAGAGTAGAGG+6.2
ZNF263MA0528.1chr2:218785675-218785696GAGGGAAGAAGGGAGAGGGGG+6.36
ZNF263MA0528.1chr2:218785703-218785724AGGGGAGGGAGGGAGAGGGAA+6.45
ZNF263MA0528.1chr2:218785723-218785744AGAGGAGAGTGGAGGGGAGGG+6.55
ZNF263MA0528.1chr2:218785707-218785728GAGGGAGGGAGAGGGAAGAGG+6.63
ZNF263MA0528.1chr2:218785755-218785776GGAGGAGAGTAGAGGGGAGGG+6.77
ZNF263MA0528.1chr2:218785711-218785732GAGGGAGAGGGAAGAGGAGAG+6.79
ZNF263MA0528.1chr2:218785720-218785741GGAAGAGGAGAGTGGAGGGGA+6
ZNF263MA0528.1chr2:218785679-218785700GAAGAAGGGAGAGGGGGAGAG+7.22
ZNF263MA0528.1chr2:218785752-218785773GGAGGAGGAGAGTAGAGGGGA+7.34
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_00005chr2:218749169-218810848Adipose_Nuclei
SE_00853chr2:218783813-218785279Adrenal_Gland
SE_00853chr2:218785303-218789553Adrenal_Gland
SE_01533chr2:218761641-218789769Aorta
SE_02835chr2:218782995-218788230Astrocytes
SE_02897chr2:218784673-218785270Bladder
SE_02897chr2:218785324-218787668Bladder
SE_03410chr2:218785503-218786601Brain_Angular_Gyrus
SE_04023chr2:218782541-218788576Brain_Anterior_Caudate
SE_05119chr2:218782590-218788342Brain_Cingulate_Gyrus
SE_05795chr2:218761584-218789646Brain_Hippocampus_Middle
SE_07532chr2:218783654-218787614Brain_Hippocampus_Middle_150
SE_08301chr2:218783392-218785231Brain_Inferior_Temporal_Lobe
SE_08301chr2:218785318-218787227Brain_Inferior_Temporal_Lobe
SE_25781chr2:218782377-218810766Duodenum_Smooth_Muscle
SE_26522chr2:218779494-218809405Esophagus
SE_31466chr2:218782600-218785265Gastric
SE_31466chr2:218785356-218789060Gastric
SE_37423chr2:218785256-218788243HSMMtube
SE_40583chr2:218761671-218809601Left_Ventricle
SE_46178chr2:218783804-218788227Osteoblasts
SE_46622chr2:218782564-218785268Ovary
SE_46622chr2:218785341-218786491Ovary
SE_47481chr2:218784801-218785153Pancreas
SE_47481chr2:218785413-218785640Pancreas
SE_47481chr2:218785702-218788090Pancreas
SE_48107chr2:218782388-218785284Psoas_Muscle
SE_48107chr2:218785313-218789348Psoas_Muscle
SE_48552chr2:218779381-218789759Right_Atrium
SE_49441chr2:218782577-218785289Right_Ventricle
SE_49441chr2:218785322-218788309Right_Ventricle
SE_50265chr2:218782546-218785298Sigmoid_Colon
SE_50265chr2:218785343-218789582Sigmoid_Colon
SE_51152chr2:218783515-218789910Skeletal_Muscle
SE_52433chr2:218782548-218785293Small_Intestine
SE_52433chr2:218785300-218789740Small_Intestine
SE_53299chr2:218761947-218789813Spleen
SE_54481chr2:218753378-218811875Stomach_Smooth_Muscle
SE_65278chr2:218780848-218785345Pancreatic_islets
SE_65278chr2:218785368-218788242Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr2218785428218786000
Number: 1             
IDChromosomeStartEnd
GH02I217918chr2218782854218789072
Enhancer Sequence
GGCAGCCACC TGTGGAAGGA ACAGAGAACG GGCAGGTGAG CATATCTTGT CTCTAGAGAC 60
AGCCAGCACC TCCTGAGGTC ACCCCACACC TCCCCCTGCT TCATTCCCTC ACACGGGCTG 120
ACACCTTCTG GGTTGAGAGT TCTTCAGCAG ACTATGGAGC AACACAGAAA AACTACTCCA 180
GCAATAACGC CTGGGAAAGG GAGCGGGGGC CGCAGAAGGC AAAAATGAAA TGAGCGTCAC 240
AATTAAAATT CTGTGACAAA TATGCACATG CTGGGAGACT GGAGATCACT GCACCGGCAT 300
TTCAATAACA GAAGCTTCAG GTAATAAGAA GAAGGATTTT TTTTTTTTTT TTTTGCTCTA 360
TGTCCTGAAT TTTCTACAAT ATGGTAAAAT TCATTTTACA TTTTTAAAAA CTGTGATTAG 420
GACCATCATC AGAAAAGGGA GAGTCACCTC CTTGGTTCTC CCCATTGCTA AGGGATCTCA 480
CCCAAAGGTC AGAGCTGCAG AAGGCTCCTA CCAGCTCTGG CACTTTCCCG GAGCATGCAT 540
GAAATGGGTT GGTAAAAGGG ACCCACCAGC CCTTCCAAAG AAAGCCATGA GTGTGGCTAA 600
CACATGTGGA AGGCTTGGAG AGGCAGAAGC ACTCTCTGGG AGTGAGCTAT GATCTTCACC 660
AGTTTCATGA TCCTCATCTT CCTCTCTGAT CCAGAGAAGG AGATGGCAAC TTGAACTTCC 720
AGACAGAGGG AAGAAGGGAG AGGGGGAGAG TAGAGGGGAG GGAGGGAGAG GGAAGAGGAG 780
AGTGGAGGGG AGGGAGCGAG AGGGAGGAGG AGAGTAGAGG GGAGGGAGGG AAGGCTCCAT 840
CGCTCCCTTC CCTGAGATAA CATTCCCCTG GCCAGGCCTG GCAGGCGAGC CATTACCCTG 900
ACAATTAGCA GGGGCATTTA TCAGAGACTG AATGTGCTCC TTTTTTCTAG CCAGGACACG 960
TTTTTCTTGG AGCTCAGTCC TCAACCTTGG CTCCGATTCC CAACCTGAAC ACCAGGCAAG 1020
GGGCCCACAG TGGGCACAGA GTGGGAGACT GTCCCTCGGG CATGAGGTTA TCTGGGAACA 1080
AGCCATGGAT GTCCAAAGAG GGGGTAGCTG CCTCCCCCAG ACAGTGGGCA ACCCCTCCCC 1140
ACCCACCAGC CCGGTGGAGT GGTGGCAGCA AGAGCCCTCA GCCCAGCCCC AGCTGGTACT 1200
GACTGGGCAT TGGGCACCCT AGCTGAGCCC TTCCTCCAGC TGACCGCATG CTGTCATCCC 1260
AGCAGCCCAG GGATTCCCCA GGCTTGACAC AGCAGCCCAG ATAAGGTCAG CACCTGTGGG 1320
ACAGTGTGCT CCAAGCTCTG GAAGGGGCAG AGGTGGCTGG GAGTTGGCAT TCCTGGGTTT 1380
TTGACACAGT CGGGCTACAG ACTCCCTGCC CAACTCATTC TCCAGCAAAG AGGCCCAAAT 1440
GGAGTCCTAG CATTTATTCC TCTTTGCTCC ACAGAATTCT AGGACTGGTG GGAGAAGAAC 1500
AGGGGGCCGA ACAGAACCAA CAACAATAAT ACCCAATACT ATTGAGTGTG TACTAGATGA 1560
CAGGCATGAT TATAAATGCT TTACCTCTGT TAACATTTTT AATCCTTTCA 1610