EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS116-16877 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr19:11205020-11207740 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
JUN(var.2)MA0489.1chr19:11205882-11205896AAGAAATGAGTCAT+7.12
JUN(var.2)MA0489.1chr19:11207063-11207077ATGACTCATTTCTT-7.12
JUN(var.2)MA0489.1chr19:11207058-11207072AGGAAATGACTCAT+8.12
JUN(var.2)MA0489.1chr19:11205887-11205901ATGAGTCATTTCCT-8.12
SREBF1MA0595.1chr19:11205756-11205766GTGGGGTGAT-6.02
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_01022chr19:11203682-11206319Adrenal_Gland
SE_01022chr19:11206333-11207663Adrenal_Gland
SE_12085chr19:11204949-11207773CD3
SE_14622chr19:11198676-11207877CD4_Memory_Primary_7pool
SE_17142chr19:11204971-11207608CD4p_CD225int_CD127p_Tmem
SE_19715chr19:11204867-11207840CD4p_CD25-_Il17p_PMAstim_Th17
SE_20994chr19:11198676-11207604CD8_Memory_7pool
SE_22774chr19:11204855-11208057CD8_primiary
SE_23239chr19:11203891-11206070Colon_Crypt_1
SE_23239chr19:11206100-11207601Colon_Crypt_1
SE_24095chr19:11204989-11205979Colon_Crypt_2
SE_24095chr19:11206366-11207012Colon_Crypt_2
SE_24095chr19:11207130-11207564Colon_Crypt_2
SE_24928chr19:11205061-11206082Colon_Crypt_3
SE_24928chr19:11206201-11206876Colon_Crypt_3
SE_26902chr19:11204916-11207828Esophagus
SE_28429chr19:11198835-11207741Fetal_Intestine
SE_29308chr19:11199027-11207595Fetal_Intestine_Large
SE_29905chr19:11204956-11208148Fetal_Muscle
SE_31737chr19:11204927-11207763Gastric
SE_34726chr19:11198191-11208606HeLa
SE_36050chr19:11204941-11207563HMEC
SE_38264chr19:11198668-11208150HUVEC
SE_40068chr19:11198411-11207591K562
SE_42817chr19:11199051-11207805Lung
SE_44493chr19:11205013-11206118NHDF-Ad
SE_44493chr19:11206328-11207705NHDF-Ad
SE_44932chr19:11205113-11207883NHLF
SE_47693chr19:11204994-11205972Pancreas
SE_47693chr19:11206368-11206786Pancreas
SE_47693chr19:11207237-11207566Pancreas
SE_49361chr19:11205119-11206191Right_Atrium
SE_49361chr19:11206197-11207709Right_Atrium
SE_50772chr19:11198863-11207767Sigmoid_Colon
SE_52540chr19:11198883-11208401Small_Intestine
SE_54059chr19:11198844-11207806Spleen
SE_57847chr19:11205007-11205595VACO_503
SE_64571chr19:11204940-11207695NHEK
SE_65732chr19:11198652-11207882Pancreatic_islets
SE_68998chr19:11207123-11207544H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr191120695311207150
chr191120569611206011
chr191120634811207740
Enhancer Sequence
CATTGGTTCA GGCTGTTCTC GAACTCCCAA CCTCAGGTGA TCCACCCGCC TCAGCCTCCC 60
AAAGTGCTGG GATTATAGGC GTGAGCCCCC GAACCCGGCC ACTCCCAGCT AAGTTTAAAT 120
TTTTTGTTTG TTTGTTCGTT TGTTTTTATT TTTTGAGACA GAGTCTCCCG CCCAGGCTGG 180
AGCGCAGATC ACTGCATCCT TGACCTCCCA GGCTTAAGCC ATCCTCCCCA CTCAGCCTCC 240
CAAGTAGCTG GGATTACAGG TGTGTGCCAC TATGCTTGGC TAAGTTGTGT ATTTTTTGTA 300
GAGATGGGGT TCAAGGGATT CTCGCTTTGT TGCCTCGGTT GGTCTCAAAC TCCTGGGCTC 360
AAGCAGTCCT CCCTCCTCAG CCTCCCAAGG TGCTGGGGAA ATCCACTTTT GAAACATTGT 420
CTGGAGAGTT GCCCAGGTGG TAGATCACAG AAATAGGTCA TCGTGGGGTC CTTCCCATGG 480
GTGCAGTCTT GAGCCACCTG TGGCCAGCAA ATATTTGGAG AATAATAGTC AGGGGAGAGC 540
TTGAGGTCCA GGGAAAGGTT TTGTTTTTCT TCAGGGAAAG GTTTTTATTG TTCTTTATCC 600
CTCCTTAAAG GACCTTCAGG TGTTACTGAC ATTCCCGGTC TACCCAGTGG CACATTTAGT 660
TTGTAAGCTG GGCCCTCGTA CAGAGGTAGG GAGGTGAGAG CATTGGATTA GTGGTCACCA 720
AAGCTGCGGT CACCTAGTGG GGTGATCAGA GGCTCCTCCC TTAAGATCTT GATTGCCAAC 780
GCCTCTGGCC CAACTTTCCT TTTTATTTAT CGCAAGCCTC CTGGAATCTC AATTGCTTTT 840
TGCCCACCCG GTGTGTCAGC ACAAGAAATG AGTCATTTCC TCCTTTAAGC ACAGTTGAAA 900
TTGAGCTGTG AGTCAGTGAG GTGTGTACGA TATTGTCAAA GCGGGGTGTG TACAGTATTG 960
ACAGATCTGT AGTTGGGCAA GAGAATTATC AGAGTTTGTG ACCACAGCAG ATTCCAAAGC 1020
TCGACTCATT TTCTTCTCTC TTCCTTCCCT TTTTTCTTTT CTTTTTTTTT TTTTTTTTGA 1080
CAGAGTCTCG CTCTGTTGCC CAGGCTGGAG TGCAGTGGCA CAATCTGGGC TCACTGCAGC 1140
CCCTGCCTCC TGGGTTCAAA TGATTCTCAT GTTTCAGCCT CCCGAGTAGC TGCAATTACA 1200
GGCATTCGGG TTCAAGTGAT TCTCCTGCCT CAGCCACCTG AGCAGCTGGG ATTACAGGCG 1260
CCCGCCACCA CGCCCGGCTA ATTTTTGTAT TTTTAGTAGA GACGGGGTTT CACCATGTTG 1320
GCCAGGCTGG TCTCGAACTC CTGAACTCAG GTGATCCGCC CACTTCGGCC TCCCAAAGTG 1380
CTGAGATTAC AGACGTGAGT CACCGCGCCC AGCCTGTTCT GTTCTTTAAT TCTCAAAACA 1440
CCCTCTAGGA AGTAGAGACT GCCATTCTCC CCCATTTTAC AGATCAGGAA ACTGAGTCCC 1500
AGAAGGATTT AGTCAGTTAC CCAAGTTGTT CTAGTTAAAT GGCCTGGAAA GCCAGTGAAG 1560
CCCAGGATTG TCTATCTAAC CCCCTTACTA CTCTAACTTT CAGGGAATCC ACATGAATGT 1620
GCTGGGTCAA CCATCAAAGT TGAAATGGAT AAAGGGGGCT GGATGCGGTG GCTGATGCCT 1680
GTAATCCTAG CACTTTGGGA GGCCGAGATG GGTGGGTGGA TTGCTTGAGC CCAAGAGTTT 1740
GAGACCAGCC TGGGCAACAT AGTGAGACAC CTGTCTCTGC AAAAAATAAA TAAAAAGTTA 1800
GCTGAGTGTG ATGGTGCACC CCTCTAGTCA CAGCTGTTGA GTTAGGCTTA GGCAGGAGGA 1860
TCGCATGAAC CTGGGAGGTG GAGGCGGCCG TGAGCCTCAG TCATGCCACT GCACTCCAAC 1920
CTGGGCAACA GAGTGAAAGC CGGTGTCCGA AAGAGAAAGA AAAAAAGACA TAGATACATC 1980
TTTTAAAGTT AGGTTGTATG TTAATTACCT ACAACTCAGT TTCAACTGTG CTTAAAGGAG 2040
GAAATGACTC ATTTCTTGCT ACATATCAAA TTAGCCCAAA ATGTAGTGGC TTAAAACAAC 2100
ACATTTATGA TTTCTCAGTT TTTGCGTGTC AGGAATTTGG AAGCAGCACA GCTAGACGGT 2160
TCCAGCTCAG GGTCTCTCAT GAAGTTGCAA TCAAAATATT GGCAGGAGAG AAAAACATAT 2220
TTTCAGAAGC TGCAGGCATA GGAAGACTTG GCTGGGGTTG AAGGATCCAC TTCCAAGATG 2280
GCGCACTCAG TGGCTCTTGG CTGGAGGCCT CAGTTCCCTG CTGCGTGGAG CTCTCCCTCC 2340
AGCTGCTTGA GTGGACTCAT GACATGCAGC TGGCCTCCCC TGGAGCAGTC GATCCAACAA 2400
TGAGCATGGC CATGAACTAG GCTCAGAAGC CACTCCCTGT CGTCTCTACA TTTTCCTATC 2460
AGAAGCAAGT CATTAAAAGT CCAGTGCCAC TCCAGGGGAG ACGAATTAGG CTCTGCCTTC 2520
TGAAAGGATT ATCACAGAAG ATGCGGTCCT ATATTCTTTT TTTAAAATTA TTCTTTTTTT 2580
TATTTTGTAG AGATGGGGTC TTGGTATGTT GCCTAGGCCA GTCTGGAATT CCTGGGCTCA 2640
AACAATCCTG TCTCTGCCTC CCAAAGTGTT GGGATTACAG GCATGAGCCA CTGCACCTGG 2700
TCATGTGGTC ATATTTTCTT 2720