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

TagContent
EnhancerAtlas ID
HS109-06028 
Organism
Homo sapiens 
Tissue/cell
Kasumi-1 
Coordinate
chr12:120668270-120670140 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxa2MA0047.2chr12:120668325-120668337GCTATGTAAACA-6.32
Foxo1MA0480.1chr12:120668329-120668340TGTAAACAGCA-6.14
RREB1MA0073.1chr12:120668626-120668646GCCCCACCCACCCCCAGCCC+6.5
ZNF263MA0528.1chr12:120668831-120668852TGAAGAGGAGGAGGATGGGGA+6.27
ZNF263MA0528.1chr12:120668834-120668855AGAGGAGGAGGATGGGGAAGC+6.79
Number of super-enhancer constituents: 55             
IDCoordinateTissue/cell
SE_00357chr12:120665596-120674461Adipose_Nuclei
SE_00799chr12:120668798-120669019Adipose_Tissue
SE_00799chr12:120669396-120669643Adipose_Tissue
SE_00942chr12:120665645-120674382Adrenal_Gland
SE_02706chr12:120666576-120671253Astrocytes
SE_06253chr12:120665302-120674513Brain_Hippocampus_Middle
SE_09726chr12:120665261-120674460CD14
SE_14823chr12:120665474-120674392CD4_Memory_Primary_7pool
SE_18785chr12:120665286-120674420CD4p_CD25-_Il17-_PMAstim_Th
SE_20423chr12:120665650-120671312CD56
SE_23304chr12:120665250-120669068Colon_Crypt_1
SE_23304chr12:120669081-120670372Colon_Crypt_1
SE_23966chr12:120665617-120668476Colon_Crypt_2
SE_23966chr12:120668513-120669009Colon_Crypt_2
SE_23966chr12:120669135-120669891Colon_Crypt_2
SE_25945chr12:120665475-120674396Duodenum_Smooth_Muscle
SE_27013chr12:120666079-120671954Esophagus
SE_27737chr12:120661321-120671266Fetal_Intestine
SE_28646chr12:120661410-120671216Fetal_Intestine_Large
SE_29635chr12:120665275-120674420Fetal_Muscle
SE_31816chr12:120665261-120671202Gastric
SE_34374chr12:120665538-120672231HCT-116
SE_34701chr12:120665310-120677162HeLa
SE_35936chr12:120665089-120674328HMEC
SE_36961chr12:120665307-120682134HSMMtube
SE_37987chr12:120665589-120684244HUVEC
SE_39166chr12:120665851-120674313IMR90
SE_40794chr12:120665283-120674362Left_Ventricle
SE_41766chr12:120665997-120669984LNCaP
SE_42203chr12:120665160-120674372Lung
SE_44237chr12:120665771-120674405NHDF-Ad
SE_44983chr12:120666343-120671286NHLF
SE_46156chr12:120666197-120674375Osteoblasts
SE_47228chr12:120657082-120682245Panc1
SE_48117chr12:120665272-120674420Psoas_Muscle
SE_48648chr12:120665717-120674244Right_Atrium
SE_50261chr12:120665247-120671947Sigmoid_Colon
SE_51208chr12:120665349-120677276Skeletal_Muscle
SE_51764chr12:120666848-120671854Skeletal_Muscle_Myoblast
SE_52496chr12:120665160-120672017Small_Intestine
SE_53419chr12:120665743-120674302Spleen
SE_54833chr12:120665944-120674285Stomach_Smooth_Muscle
SE_55411chr12:120666987-120671131Thymus
SE_55760chr12:120665089-120669338u87
SE_55760chr12:120669368-120674418u87
SE_56964chr12:120665382-120671190VACO_400
SE_57600chr12:120666271-120668537VACO_503
SE_57600chr12:120668579-120669951VACO_503
SE_58043chr12:120665341-120669936VACO_9m
SE_63549chr12:120666328-120674360HSMM
SE_64693chr12:120666407-120670770NHEK
SE_65557chr12:120665412-120671336Pancreatic_islets
SE_67501chr12:120665089-120669338u87
SE_67501chr12:120669368-120674418u87
SE_68908chr12:120665403-120671309H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12120669025120669761
Enhancer Sequence
GCCCACGCTC AGGGATATAA GCAGTGAGCA GGGCTTGGCC CTTCCTAAGG AAGGAGCTAT 60
GTAAACAGCA GGACCAGCTC AGGGATGGTC TCATCTCAGC CCCTTTGGTG AGACTCTTCC 120
AGATTAGGAA GGAAAACAGA ACGGGAAGGC GGGTCTCCCC CCTCCCCCTG GCTCCAAGTT 180
CCCCTCCCCT CCCCCAGCCC AGAGCACATG AGCAGTTAGA GCAGAGGTAA TCTAATCCGC 240
AGCGGGGTGC TTTCACTCGG TGAGTAAGTC CCCAGGAATG GTGAGCTGGG TATATTTATC 300
CTGATAACCG TCTGTCCTCA GTAAGGGCCA ATCCACAATT AGGCCAGATC CACTCTGCCC 360
CACCCACCCC CAGCCCAGGG ACCTAGGGCC TGGACACTGA CTAGGAACTC AGTCTCCTTG 420
AGGGGCCTTC CCTGCCAATT TGGGTTCTTG TCAACTGTCT CCTCTCCAAG AATTAAGCTC 480
CAGAGAGCAG GGGCCTTGTC GGTCTTGTTC GATGCCATAT CCCCAGCAGC TAGAATGAAT 540
GGCTGAATGA CAGAGGGGCT GTGAAGAGGA GGAGGATGGG GAAGCAGCAG TGAGCAGAGC 600
AAACAGCCAG TGCGGAGGAG GGGAGCCAGG ATGCCCTGAT CCCAGGCCCA GCGGATGAGT 660
GGGGGCCCCT CAGCGGATCC TCTAACCTCT CTGGATGTCT TCTCTATCAA GAAAATGGGC 720
AGAACCCGAT TTGTCCCCAT TCCTAGTAGC ATGCTCTGAG GAGATAATAC AATTATGGGT 780
GAGATTTATA TAGCACCTTT GAGCTCTTCC GAGTTAGTCT AAATCCAAGA TTCTGCTATT 840
ATCTGAATCC CAGACAGGAA CTGCTCTGCT AAGAGGATGG ATGAGAAACG ATCAATACCA 900
TAGTGTCATT TAAATATTTA ATAGCCATGC CTGGAGGTTA CAAAGACTCA GCCACCAATT 960
CTCCTCCGCT GACTCATGCC TCACTCAACA GGAACTGCAT TTTACCCTTA CAGCCCTGAA 1020
GGAAGTGTGG GCTGGGGGGT GACACACAGG AAGCCAGGGG AGAAGGCCCA GGAGTCTTCC 1080
AGTCAGCCGC CAGGGGAGGA GGGGGTGGTC ATTTGGATGA AGTGGTTCTT CCCCAGGCTT 1140
CCTACAGGCC TAGCTTAGGA GGGTGGCTTC CTGTATGCTG AGGAGCTCTT CCTTGCAGAG 1200
GGTGACACAA TATGAGTGTG CAGACAGACT GGCTTTATTG GCTGCCTGGC TTGTGCCCAA 1260
GGTCACAGGG CACAGGTAAC CAGAGACCTG AGAAAATAAT GGCTGCAAGG CAACTCCAGC 1320
AGTCACCCTG AGCTCCAGGC AGAAGACCAA CTGTGCCAGG CCCATCTGCA CCAGGCACAC 1380
ACAAGGCCCA CCCATCAGGC TCCTGGCTGC AGCCACTTCC CCATCAAATT GGGCTCCAGG 1440
AGCTTAAGCA ACAGCAGGTG AGACAAGGCT GCCCAGGTTG ACTCTGAGCA CTTCTATGCA 1500
TCTGCCTTAG GCTACAGACA CAGGAGTTCA GGCCAGGCTG GCCAAACACC AGAGTCTTTC 1560
TCTTCTTTTT TTCTTTTTTT GAGACAAGTC TTGTTCTGCC ACTCAGGCTA GAGGCCTGAT 1620
CACAGCTCAT TGCAGCCTAG AATTCTTGGG CTCAAGGGAT CTTCCTGCCT CAGCCTCCCG 1680
AGTAGCTAGG ACTAAAAGCA CATGCCACCA CACTAGGCTT TTAAAAACTT TTTTGTAGAG 1740
ACAGGGTCTC ACTATGTTGC CCAAGCTGGT CTTGAACTCC TGGCCTCAAG CCATCTTCCT 1800
GCCTGGGCCT TCCCAAAGTG CTGAGATTAC AGACAGGAGC CACCATGCCC ATCCCCAGAG 1860
TCTCTTTCAT 1870