EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS176-19000 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr19:39221860-39224340 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Klf1MA0493.1chr19:39223325-39223336AGCCACACCCA+6.14
Sox6MA0515.1chr19:39222320-39222330AAAACAATGG-6.02
TFAP2CMA0524.2chr19:39222611-39222623TGCCCTCGGGCA+6.27
TFAP2CMA0524.2chr19:39222611-39222623TGCCCTCGGGCA-6.52
Number of super-enhancer constituents: 42             
IDCoordinateTissue/cell
SE_00117chr19:39223455-39224893Adipose_Nuclei
SE_00865chr19:39221827-39223103Adrenal_Gland
SE_00865chr19:39223179-39226384Adrenal_Gland
SE_01543chr19:39221172-39222920Aorta
SE_01543chr19:39223170-39226331Aorta
SE_03903chr19:39222331-39223034Brain_Anterior_Caudate
SE_03903chr19:39223399-39224458Brain_Anterior_Caudate
SE_04868chr19:39221898-39222989Brain_Cingulate_Gyrus
SE_04868chr19:39223257-39226211Brain_Cingulate_Gyrus
SE_05805chr19:39220864-39226369Brain_Hippocampus_Middle
SE_06803chr19:39223258-39224775Brain_Hippocampus_Middle_150
SE_07777chr19:39221561-39224896Brain_Inferior_Temporal_Lobe
SE_23062chr19:39221124-39223041Colon_Crypt_1
SE_23062chr19:39223139-39226383Colon_Crypt_1
SE_23732chr19:39221141-39223030Colon_Crypt_2
SE_23732chr19:39223159-39226349Colon_Crypt_2
SE_24739chr19:39221166-39222992Colon_Crypt_3
SE_24739chr19:39223124-39226357Colon_Crypt_3
SE_26525chr19:39221655-39226384Esophagus
SE_27614chr19:39217995-39226375Fetal_Intestine
SE_28533chr19:39216812-39226417Fetal_Intestine_Large
SE_31384chr19:39218125-39226350Gastric
SE_34299chr19:39223246-39226335HCT-116
SE_36926chr19:39223908-39225843HSMMtube
SE_40594chr19:39221759-39226363Left_Ventricle
SE_41601chr19:39221200-39223057LNCaP
SE_41601chr19:39223113-39223637LNCaP
SE_41601chr19:39223936-39224524LNCaP
SE_42097chr19:39221138-39226370Lung
SE_46686chr19:39223870-39224361Ovary
SE_47114chr19:39164477-39226374Panc1
SE_47461chr19:39221191-39223035Pancreas
SE_47461chr19:39223112-39223741Pancreas
SE_48555chr19:39223100-39224757Right_Atrium
SE_50056chr19:39221079-39226331Sigmoid_Colon
SE_51136chr19:39221894-39222970Skeletal_Muscle
SE_52339chr19:39221091-39226335Small_Intestine
SE_53291chr19:39215486-39226355Spleen
SE_54534chr19:39223068-39224526Stomach_Smooth_Muscle
SE_56725chr19:39221125-39223036VACO_400
SE_56725chr19:39223151-39226345VACO_400
SE_65266chr19:39219871-39226337Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr193922224439222983
Enhancer Sequence
AGCCTAGGGG GAGGCTGCTT CTGAGCCCAG TGGCCCACAG GGAACCCACC TTGGCATTGC 60
ATCCCCACCC CACCTCCTCA GGGAGGACAT GAATGCCACA GGGTGTCACA CCCCAACTCT 120
GCCCCATCCC GGCAGGGTGA GTACAGGCTG ATCCCTTCAA TCCTCTGGGC CTGTTTCCTC 180
ATCCATCAAA CGGACTAAGA CAGCCCCGAC CCCATAGGGT GTGTGAAGAC AGAACGCTCA 240
GGACAGCGTC TGACACGTGA CTCGATGTGT GGGTACTGTT ACTCCTTAAA TCCTGTGGGG 300
CTTTCTCCTT GCCAGTGGGC ACTGGAGGAT ATTTCTGTGC AGCAAAAAAT ATAGTCAATC 360
CCATATGGAG TCAGTTTCCT TACAGTCTAC CTCAGAGGCG ATTTCTAAAG CTGAGAAACC 420
ATGTCTGCTG TGGAGTCTCA TTGGAGGCTT TTAAAAACCC AAAACAATGG GTTCTTGACC 480
CCTTCTGAGA TGCAAGGTTG TGCCTGATGA CCTTTGTCTC CCACACGGCC AGACAAACCC 540
AGTTCCAAGT ACCGTTTCAT GGGCTTCTGC TGCTTCCAAA GCCCATCTTC ACCCCCATTC 600
TGTGTGTTCA TTCTCTTCAC AAATATCTAC CAAGTAAGTG CCATTTCATG CTGTGCCCAG 660
TGCCAGGTGC TGTTTTAACA GGAGGGCAGG TGGCCTGCAG CCTCTTCCTG CCCGTGTGAC 720
CTGCCCCAGG TCACTCCCTC TGGCATTCAT CTGCCCTCGG GCATAGGGGT GGAGGCTGCC 780
ATGCCCAGGG CTATGGGGAA ACCCAGCCAG ATGGGGTGGA AGGACCCGAG AAGGCGCTGG 840
AGCCCCTCAG CTGCCACTGC AGGAGTTCCC GTTTGAGAAA TTCTCAAGGG CACTTTATCA 900
GTTTCCTTCT TCCTGGAATA ACTCCTGGCA TGTAACAGGC ACTCACTGGT GCCAGATGCG 960
TGAACACAAG CCTGCCACCT GCCACCTGCT GTGAGTCCTT GCTCCCTCAC CTCCACTCCT 1020
GTCTATCTCC GGCCCAGCCT CTCCCTCTCT GCCCCACGTC TCCCAATCCT TGGCTGTCTC 1080
TGACCCCATT TCTCCCCCTT TGACTTGGGC TTTTTCTTTT TTCTTTTTTG AGACGGAGTC 1140
TCGCTCTGTT GCCCAGGCTG GAGTACAATG GCATGATCTT GGCTCACTGC AACCTCCACC 1200
TCCCGGGTTC AAGAGATTCT CCTGTCTCAG CCTCCCAAGT AGCTGGGATT ACAGGCACGC 1260
ACCACCACGC CTGGCTAATT TTTGTAGTTT TAGTAGAGAC GGGGGTTCCG CCATGTTGCC 1320
CAGGCTGGTC TTGAACTCCT AGGCTCAAGC AATCTGGCAA TCTGCCTGCC TTAGCCTCCC 1380
AAAGTGCTGG CATTACAGGC GTGAGCCACC ACGCCCGGCT GGCTCTTTTG GACACTTGAC 1440
CACCTTCTCT GGGTCTCACA CTCACAGCCA CACCCAAACC CTCTCCCTCT GGCTCTCCGA 1500
CTCCATCACA GTCACCCCAG CCCCCATCTC CCTGTGGCTC CATCTGCTGT GTGGTGGCAG 1560
ACAGGCCCCA GAGTGGGGTT GGGGATCTGG GAACTCCAAG TTCTGACCCC AGCCCACTCT 1620
CCAAATCCCC TCCACATGAG GGTCACAGTG CTGTACTGTC TCATCTGCCT TGGAGCCCAT 1680
GGAAAGCCTT TCTCTCTGGC TCTCTTTCTT GGTTAGGATG TTGTGCTGGG CTTGTTCCAG 1740
CTCATCAGGA GGAACTCAGC CTAGTAGCAG AGGCCATTGG CCGGCTCTCT TTGGGGCTTT 1800
TGGTAATGAA AGCTGCATTC TCCAATCACT AAGTGCTATG CCCTGCAGTG CATGGACGAC 1860
TCCTCACCAC CCTGTGTACT AGCTTTTTTT TTTTTTTTTT GAGAGGCAGG CTCTTGCTCT 1920
GTCACCCAGG CACAATCACG GCTCACTGCA GCCTCAGCCT CCCGGGCTCA AGCCATCCTC 1980
AAGCCTCAGC CTCCTGAGTA GCTGGGACCA TAGGTGTGAG CCACCACACC AGGCCCTGGC 2040
CATTTTAGAG AGGAAAATGG AGGCTCAAAG AGATGAAGTC AAGTGCCCAG GGCCCCTCCT 2100
GGAGTCAGTA GAGTGAGGAT TCCAACCCCG GTGCACCAGA ATCCAGAACA TTCTACCATG 2160
CTGCCCTGGG GGCCAGACCC TCTCAGATAC CAGCTCCTAA TCTTCCCCTT CCTGGAGGGG 2220
CCTCTCCCTG CCCCAGAACC CCTACCAGGC ACATCCCCCT TTCATGTCCT CCCCACCCCA 2280
CACACGCCCC TTGCCCTTCT CCTTCCTTAT TTGGCCTCTT TCAGGGTCAC CCAACCCCTG 2340
CCAGGGACTG GCAACAAGCT AAGGTGTGGG CCTGTGGATG GCCACAGTGC AGACGGCCAC 2400
AGCTGAGCAG GGGGACTTGG AGACAATGGG ATGGGAGAGA ACAGGTCCTG TCCCCACGAC 2460
CACCCCAGGA CCCTGTCCAC 2480