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

TagContent
EnhancerAtlas ID
HS176-42817 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr9:130301170-130303820 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HEY2MA0649.1chr9:130302791-130302801GACACGTGCC+6.02
IRF1MA0050.2chr9:130301229-130301250AAAAAAAAAAAGAAAGAAATG-6.04
Npas2MA0626.1chr9:130302791-130302801GACACGTGCC-6.02
ZNF263MA0528.1chr9:130303294-130303315GGAGGTGGGGGAAAGAGGGGG+6.56
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_00872chr9:130301362-130305061Adrenal_Gland
SE_01693chr9:130301447-130305093Aorta
SE_02373chr9:130301275-130303274Astrocytes
SE_02928chr9:130302798-130303441Bladder
SE_06387chr9:130302332-130304635Brain_Hippocampus_Middle
SE_25019chr9:130302815-130303578Colon_Crypt_3
SE_26215chr9:130301070-130302527Duodenum_Smooth_Muscle
SE_26528chr9:130301222-130305101Esophagus
SE_30306chr9:130301242-130302023Fetal_Muscle
SE_31422chr9:130301413-130305092Gastric
SE_34621chr9:130301868-130303210HeLa
SE_36116chr9:130302619-130303876HMEC
SE_37370chr9:130296708-130303020HSMMtube
SE_37370chr9:130303549-130309613HSMMtube
SE_38118chr9:130300999-130306708HUVEC
SE_39322chr9:130301374-130303109IMR90
SE_41594chr9:130301481-130302214LNCaP
SE_41594chr9:130302280-130304532LNCaP
SE_42140chr9:130301360-130305141Lung
SE_44201chr9:130301106-130305134NHDF-Ad
SE_44773chr9:130301229-130303604NHLF
SE_45705chr9:130295920-130309670Osteoblasts
SE_46654chr9:130301468-130302741Ovary
SE_47421chr9:130298734-130303006Panc1
SE_47421chr9:130303426-130305379Panc1
SE_47474chr9:130301585-130303600Pancreas
SE_50184chr9:130301266-130305116Sigmoid_Colon
SE_52096chr9:130301237-130303157Skeletal_Muscle_Myoblast
SE_52507chr9:130301408-130305027Small_Intestine
SE_53712chr9:130301439-130302968Spleen
SE_54748chr9:130301339-130309339Stomach_Smooth_Muscle
SE_55718chr9:130301051-130305145u87
SE_63440chr9:130298563-130342452NCI-H69
SE_63712chr9:130301223-130303171HSMM
SE_64980chr9:130302475-130303818NHEK
SE_65259chr9:130301019-130309850Pancreatic_islets
SE_67516chr9:130301051-130305145u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr9130301377130302914
chr9130303291130303601
chr9130302644130303276
chr9130303698130303793
Number: 1             
IDChromosomeStartEnd
GH09I127533chr9130295863130309594
Enhancer Sequence
CTGAGATTGC GCCATCGTAC TCTAGCCTGG GAGACACAGT GAGACTCCAT CTCAAAAAAA 60
AAAAAAAAAA GAAAGAAATG CAGTTGTGAT CACATCTGGA ATTCACTATA TACTTAAAAT 120
GGATAATTTA TACAAAGACT GTGTATTAGG GACATCTCAT AGTAAGAAAA ATTAAGGATC 180
GAGCTGACTG ATCTTTTGGG AATGATAGAT ATGTGGAAAA ATACAATAAA GATCTAATTT 240
GGGTCAGTCA AAAAAAAAGA AAGGAAGAAA AGTGAGGCTC AGAGAGACTC ACTGACTCAC 300
TCAAAGACAC ACAACGGAGG GGAAAGAGGT GGGTTTTGGA CCTTGTCTCC CACCAAAGCC 360
TGCACAGAGC CCTACCCCGC AAAGCCTCTC ATCCCAGTGA CCCCTCACGA GGACCCGCAA 420
TGCCGCTTTC AAACCCCTGG TTTTCCACTC TCTTGCTGGG GTCTTGCCCA ATCCCAAGAA 480
TGAGGCAACA CAAGGCTTTA CTATCCTCAT CTTACAGACG AGGAAACCGA GGCTCAGAGG 540
GCAAAGTGAC TTTCCCGAGG CAACAGCTGG CAGGTGTCAG AGCCGGGACT GAGGTCTAGG 600
GTTTCCAGCT CCACTGGCCC CTGTCGGGTC GGAGCTGGTG GAGAATCATC CGACCCACTG 660
GAGCCTTACT TCTTCATCCT CACTGGGCCC TAATTTTCCC ACCTTTAAAA TGGGAGGGTG 720
GGTCCCTGTC AGCTCAGCTG ACCGAAAATC TCAACGACAA TCTAATCAGT GCTGCCCTGG 780
CCCCAGGAAC TGACCGGGAT GCTGGCCTCA GCCCCTCCTG TGAGCTGCTG GTGAGTCAGC 840
TCTGACCAGC AGCTGATCAC AGCCCCCTCG GGCCAGACAA AAGGACCCGG GGGGAGAACT 900
AGGCACCCCC CATCACCTGC AAACAGGGCA CCATTTCTAC ATGGACACAC AGGCTCTGGG 960
TCCAAGTCCC AGCTCTGCCA CCTATGAGCT GTGTGGCCTT GGCTAAGGCA CTTCTCCTCT 1020
CTGAGCCTTT ATTTTCCCCT CTGCAAAATG GCACAACAGT ATCTGCCTGA ATGGGTTATG 1080
AGACAAACGG GCTACTGAGC ATGAAGCCCT TTACCCTGGC AAGAAGGGGG CACTTCACCA 1140
ATGGGGGCTC CTAAGAAGTG CCTCTTGTCA AGGTTCCTCT AACCCACAGT GAGGCCCTTG 1200
AAACAGAGGC TGAGCATGCA GCCTGGCCCA CCCTGGGACC AGCTCCAACA GCAGCCAAGG 1260
CGGCCGGAAC GTTAATTAAT CTCTGATTTT CCAAACTGAC AACGTTAAGG GCCACGCTAC 1320
TTCCTGTGCA GATAGTGAGG CTGGGCAAGA ACTGGGGAGG CCCCAGGGTG GCCTGGAGGC 1380
TTGGGGAGCT GGGGGATGGG GTACCAGGCC CACTGTGCAG ATAGGGGAAC TGAGGCTCAG 1440
AGAGGAGAGG AGGCTTGCTG AGCTGAGAAT GGAGGAAGGA GTCCAGGGGT TCTCAGAAAA 1500
TGGACCTAAA AAGGCGTATC CCGGAGGGCC TCGAATGCCA AGCTAAGGAG TTCCTTCTTT 1560
GCCTTGTCAT GACGCTCCCC AAAGCCACCA TGTGCCGCTC CTGTGCTAAG CATTTTGCTT 1620
GGACACGTGC CCCCGATTCT TCAACTCAAC CTCGGGCCAG GTGGTATTGG TACTGGCAGA 1680
ACATTTCAGA CCAGGTGACC GAGAACTGGG TACCTCTGCC AAATCACTCT GCTGAGAAGA 1740
GGCAGAGGTA GGATCTGCAC CCTGGTCCCG ACCTGATGCC TAAGCCTGAA ACCCTGTTCC 1800
ACACGGACGG GGGACCCAAG AGGAAGAGAG TCATCTCCAG CTGCGACCAC ATCCAGCTCA 1860
TGTCCACCAT GGGGGCTGCA CGCCGGCGCC AGCCCTGGTT TGGCCCCAGT GGAGGGCGCT 1920
GTGCCAGACC CGTTCCTGGC TCATCCGGTC TCTCCAGTGG GCTCCAGGGA CACACCTCAC 1980
CCACGAGGCC CAGCCCGGTT TCAGGGTTTC AGGGCTGAGA GGTTTGCCGA CTGAAACCAG 2040
GCAGGTAGCA GCACCCTGTA GGGTGGGGCA GGCTCAGAAC CTGCCCGCCT GGTTCCCAGG 2100
GCATAGGGAG CAGGTCCAGC ATGGGGAGGT GGGGGAAAGA GGGGGGTGCC GACCCCACCC 2160
ACCCTACAGT CCAGGGACCA GCAGAGGCAG AGTCGGGGCA GGGACTCCAT TCTCGCAGGT 2220
CTCAGAGTTG TCCCAAGCAC CACCATCTCC ATCATGTGCC TGAGACAGCA GGGAGAGCTT 2280
GGGGTCCAGA AAGGTGGTGA CACTCTCCTA GGGCCACACA GCACATCCAA CAGAGCTGGG 2340
TTGGCATAGA CCAGTGCCTC GCTCAGGGCC TTTCTACTTT CTACTTGCCC CCCACCTACT 2400
GTCACAATCG ACACACAATA GCAGCAGCCA CTTGTCAGCA CCACCTCTGT GCCCAGCACG 2460
GCACTGCACA TGCACACTCA TTATTTCACG CACTGTCCTC ACTTCCCAGA GAACACTGAG 2520
GCTCAGAGAG GTTAAGGGAC TTCTCCAGGG ACACACAGCT TGTAAATGAC ATGAACTCTG 2580
AACAGGGAAC CAACGTTTGG GCAAAACCAT CTCACCCTGG CCTCCGCAGC ACCAGCCTGT 2640
GGGTGGCCTC 2650